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Cited 30 time in webofscience Cited 33 time in scopus
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dc.contributor.authorChung, SK-
dc.contributor.authorLee, JM-
dc.date.accessioned2016-03-31T13:41:31Z-
dc.date.available2016-03-31T13:41:31Z-
dc.date.created2009-02-28-
dc.date.issued1999-04-23-
dc.identifier.issn0957-4166-
dc.identifier.other1999-OAK-0000000766-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/20391-
dc.description.abstractSerine was efficiently converted to the N-p-methoxybenzyl (PMB) protected alpha'-amino enone derivative 6, which was reduced with Zn(BH4)(2) to the corresponding anti-beta-amino alcohol in >96% de. On the other hand, N-PMB-N-Boc-protected alpha'-amino enone derivative 8 was reduced by NaBH4 to syn-product with a diastereoselectivity of ca. 90%. (C) 1999 Elsevier Science Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfTETRAHEDRON-ASYMMETRY-
dc.subjectD-ERYTHRO-SPHINGOSINE-
dc.subjectD-THREO-SPHINGOSINE-
dc.subjectASYMMETRIC SYNTHESES-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectEMMONS REACTION-
dc.subjectCELL-ADHESION-
dc.subjectACIDS-
dc.subjectALPHA-
dc.subjectREDUCTION-
dc.subjectALDEHYDES-
dc.titleStereoselective synthesis of beta-amino alcohols: practical preparation of all four stereomers of N-PMB-protected sphingosine from L- and D-serine-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1016/S0957-4166(99)00147-0-
dc.author.googleCHUNG, SK-
dc.author.googleLEE, JM-
dc.relation.volume10-
dc.relation.issue8-
dc.relation.startpage1441-
dc.relation.lastpage1444-
dc.contributor.id10200284-
dc.relation.journalTETRAHEDRON-ASYMMETRY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationTETRAHEDRON-ASYMMETRY, v.10, no.8, pp.1441 - 1444-
dc.identifier.wosid000080753100005-
dc.date.tcdate2019-01-01-
dc.citation.endPage1444-
dc.citation.number8-
dc.citation.startPage1441-
dc.citation.titleTETRAHEDRON-ASYMMETRY-
dc.citation.volume10-
dc.contributor.affiliatedAuthorChung, SK-
dc.identifier.scopusid2-s2.0-0033597395-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc29-
dc.type.docTypeArticle-
dc.subject.keywordPlusD-ERYTHRO-SPHINGOSINE-
dc.subject.keywordPlusD-THREO-SPHINGOSINE-
dc.subject.keywordPlusASYMMETRIC SYNTHESES-
dc.subject.keywordPlusORGANIC-SYNTHESIS-
dc.subject.keywordPlusEMMONS REACTION-
dc.subject.keywordPlusCELL-ADHESION-
dc.subject.keywordPlusACIDS-
dc.subject.keywordPlusALPHA-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordPlusALDEHYDES-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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