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PARK, JAIWOOK (박재욱)

Dept of Chemistry(화학과)

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SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROGENEOUS OXIDATION:2||HETEROSTRUCTURES:2||AU:2||ruthenium complexes:2||BOWLSHAPED PHOSPHANE:2||alcohols:2||PHOTOCATALYTIC DEGRADATION:2||POLYISOPRENE:2||LEWISACIDS:2||ENANTIOMERICALLY PURE:2||EQUILIBRIA:2||SYSTEMS:2||ORTHOLITHIATION:2||HIGHMOLECULARWEIGHT:2||POLYMERIZATION:2||BIPYRIDYL4,4&apos:2||enzymemetal combo catalysis:2||chirotechnology:2||TRANSITIONMETAL NANOPARTICLES:2||RADICALMEDIATED RACEMIZATION:2||RECEPTOR:2||ALZHEIMERSDISEASE:2||DIRECT ALPHAALKYLATION:2||PROPARGYLIC ALCOHOL DERIVATIVES:2||RADICALCHAIN REACTIONS:2||IDENTIFY:2||NH imines:2||Pdcatalysts:2||allylation:2||AROMATICAMINES:2||chemoselectivity:2||DKR:2||ENZYME IMMOBILIZATION:2||TEMPERATURE:2||LIQUIDCHROMATOGRAPHY:2||BUILDINGBLOCKS:2||FORMAMIDE:2||SULTAM:2||CONVENIENT METHOD:2||DERIVATIVES:2||OXAZOLINES:2||XRAY DIFFRACTION:2||VISIBLELIGHT:2||ATMOSPHERIC OXYGEN:2||FLIGHT MASSSPECTROMETRY:2||Gold nanoparticle:2||REDUCTION:2||Aerobic alcohol oxidation:2||radicals:2||PALLADIUM COMPLEXES:2||METALCOMPLEXES:2||substituted oxazolinylferrocenes:2||N,P &apos:2||Adenosine triarsenate:2||AIR OXIDATION:2||RATE ENHANCEMENT:2||lipases:2||NICKEL:2||ELECTRON INJECTION:2||CARBONDIOXIDE:2||HYDROXY ACIDDERIVATIVES:2||DIOLS:2||polystyrene:2||SYNTHETICPOLYMERS:2||POLYSTYRENE:2||ODONORS:2||ACYLTRANSFERREACTIONS:2||ABINITIO:2||POLYSILANE:2||EVOLUTION:2||SOLARCELLS:2||CURRENTDENSITY:2||HYDROXY ALDEHYDES:2||HETEROGENEOUS CATALYSTS:2||CONVERSIONS:2||CC bond formation:2||SECONDARYAMINES:2||photolysis:2||RHODIUMCATALYZED HYDROGENATION:2||CHIRAL BRONSTED ACID:2||chelate:2||DIPHENYLPHOSPHINO(OXAZOLINYL)FERROCENE LIGANDS:2||1,1&apos:2||Energy carrier:2||ADPARSENATE:2||PARTICLES:2||GRADIENT:2||SILANES:2||hydrosilylation:2||CARBONYLCOMPOUNDS:2||HINDERED KETONES:2||ADSORPTION:2||racemization:2||IONIC HYDROGENATIONS:2||HYDRIDE TRANSFER:2||TRANSFORMATION:2||CRYSTALSTRUCTURE:2||ENERGIES:2||CRYSTAL:2||NANOSTRUCTURED SEMICONDUCTOR PHOTOELECTRODES:2||(2,2&apos:2||asymmetric transformation:2||GRADIENT INTERACTION CHROMATOGRAPHY:2||HYDROXYAPATITE:2||NANOCLUSTERS:2||alkynes:2||HYDROSTANNYLATION:2||INDUCTION:2||isomerization:2||POTASSIUM ALKENYLTRIFLUOROBORATE SALTS:2||CANDIDAANTARCTICA LIPASE:2||HYDROLYTIC OXIDATION:2||NANOCATALYSTS:2||INDOLES:2||enamides:2||UNSUBSTITUTED IMINES:2||1 &apos:2||PSEUDOMONASSTUTZERI LIPASE:2||AMINOALLYLATION:2||AMMONIA:2||FE3O4:2||RACEMIZATION CATALYST:2||ASYMMETRIC REDUCTIVE ACYLATION:2||hydrogenation:2||STABILITY:2||CARBONATION:2||CATALYTIC REDUCTION:2||FERROCENE:2||BEHAVIOR:2||ONEPOT SYNTHESIS:2||POLYDISPERSITY:2||HYPERPARATHYROIDISM:2||Heterogeneous catalyst:2||Room temperature:2||hydrostannation:2||EFFICIENT SYNTHESIS:2||SUBSTITUTED ENAMIDES:2||azides:2||HOMOALLYLIC AMINES:2||oxidation:2||PLATINUM:2||aldehydes:2||FILMS:2||CYCLOADDITIONS:2||PLANAR CHIRALITY:2||FERROCENES:2||SILICON:2||DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEXES:2||RUTHENIUM(II) COMPLEXES:2||NANOPALLADIUM CATALYST:2||HETEROGENEOUS CATALYST:2||STILLE CROSSCOUPLINGS:2||CHIRAL BISPHOSPHINE LIGANDS:2||BIDENTATE NITROGEN LIGANDS:2||ENANTIOSELECTIVE CATALYSIS:2||ruthenium catalyst:2||synthetic method:2||ASYMMETRIC HYDROGENATION:2||ENOL TOSYLATES:2||allylic substitution:2||Arsenic:2||imines:2||TIBETA:2||LIGAND:2||CONVENIENT:2||OH RADICALS:2||DIRECTED EVOLUTION:2||CHEMICAL MODIFICATION:2||ASYMMETRIC ALDOL REACTION:2||POLYMER:2||AMINATION:2||PD:2||TRANSFORMATIONS:2||POTENTIAL CHARACTERISTICS:2||POLYPYRIDYL COMPLEXES:2||catalytic racemization:2||PRACTICAL ROUTE:2||SOLVENTFREE OXIDATION:2||SECONDARY ALCOHOLS:39||DYNAMIC KINETIC RESOLUTION:26||RACEMIZATION:25||AMBIENTTEMPERATURE:20||PALLADIUM:19||ASYMMETRIC TRANSFORMATIONS:17||ENZYMES:17||COMPLEXES:16||LIPASE:15||COMBINATION:13||KETONES:13||METAL:11||ENZYMATIC RESOLUTION:10||ruthenium:10||HYDROGENATION:10||EFFICIENT:9||ALDEHYDES:9||RUTHENIUM COMPLEXES:9||ROOMTEMPERATURE:9||CHIRAL ACETATES:8||ALCOHOLS:8||ENOL ACETATES:8||ORGANICSOLVENTS:7||WATER:7||ALLYLIC ALCOHOLS:7||RACEMIZATION CATALYSTS:7||AMINES:6||NANOPARTICLES:6||OXIDATION:6||CHIRAL AMINES:6||CATALYSTS:6||RUTHENIUM:6||HYDROGENTRANSFER:6||PSEUDOMONASCEPACIA:5||SELECTIVE OXIDATION:5||METAL CATALYSIS:5||EFFICIENT ROUTE:5||heterogeneous catalysis:5||dynamic kinetic resolution:5||ENANTIOMERICALLY PURE AMINES:5||ALLYLATION:4||ANIONICPOLYMERIZATION:4||TITANIUMDIOXIDE:4||TRANSITIONMETAL COMPLEXES:4||ACTIVESITE MODEL:4||HYDRIDE:4||PRIMARY AMINES:4||OPPENAUERTYPE OXIDATION:4||ENZYME:4||CATALYST:4||MOLECULAROXYGEN:4||MECHANISM:4||photochemistry:4||NANOCRYSTALLINE TIO2:4||IONIC LIQUIDS:4||PHOSPHINOARYLOXAZOLINES:4||HYDROLYSIS:4||ENANTIOMERS:4||ENANTIOSELECTIVE HYDROGENATION:4||REAGENTS:4||ORGANICSYNTHESIS:4||ASYMMETRICSYNTHESIS:4||ENANTIOMER:4||ACYLATION:3||LIGANDS:3||ENANTIOSELECTIVITY:3||ALCOHOL REACTS FASTER:3||BACKBONE:3||MILD CONDITIONS:3||SUBSTITUTION:3||ISOMERIZATION:3||COUPLING REACTIONS:3||catalysts:3||RUTHENIUM CATALYSTS:3||CATALYTIC RACEMIZATION:3||ALKYLATION:3||ACID:3||LITHIATION:3||BIS(OXAZOLINYL)FERROCENES:3||POLYMERS:3||ESTERS:3||CYCLOPENTADIENYL:3||METAL COMBO CATALYSIS:3||ETHERS:3||palladium:3||ENANTIOSELECTIVE ACYLATION:3||HIGH INITIAL ACTIVITY:2||temperature gradient interaction chromatography polystyryllithium:2||ALPHACHYMOTRYPSIN:2||FERROCENYLPHOSPHINEGOLD(I) COMPLEX:2||CYCLIZATION REACTION:2||QUATERNARY CARBON CENTER:2||ATP:2||CROSSCOUPLING REACTIONS:2||HETEROG