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  Department of Chemistry (화학과) 1. Journal Papers

 

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Cited 7 time in webofscience Cited 10 time in scopus
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dc.contributor.authorKang, S-
dc.contributor.authorKim, DG-
dc.contributor.authorRhee, YH-
dc.date.accessioned2016-03-31T07:35:26Z-
dc.date.available2016-03-31T07:35:26Z-
dc.date.created2015-02-07-
dc.date.issued2014-12-01-
dc.identifier.issn0947-6539-
dc.identifier.other2014-OAK-0000031807-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/13797-
dc.description.abstractA highly efficient and stereoselective synthetic pathway towards trans-3,4-dihydroxy-2-alkylpyrrolidines and piperidines is described. The nature of the protecting groups on the hydroxyl moieties played a crucial role on the trans selectivity. By using this method, a concise total synthesis of (-)-2-epilentiginosine has been achieved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherWiley-VCH-
dc.relation.isPartOfCHEMISTRY-A EUROPEAN JOURNAL-
dc.subjectdiastereoselectivity-
dc.subjectenantioselectivity-
dc.subjectheterocycles-
dc.subjectnatural products-
dc.subjectsynthetic methods-
dc.subjectN-ACYLIMINIUM IONS-
dc.subjectOXOCARBENIUM IONS-
dc.subjectEFFICIENT SYNTHESIS-
dc.subjectDERIVATIVES-
dc.subjectINDOLIZIDINES-
dc.subjectNUCLEOPHILES-
dc.subjectALLYLATION-
dc.subjectINHIBITORS-
dc.subjectCHEMISTRY-
dc.subjectAMINES-
dc.titleAccess to trans-3,4-Dihydroxy-2-alkylpyrrolidines and Piperidines by Use of Stereodefined Cyclic N,O-Acetals as a Diversity-generating Element-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1002/CHEM.201404659-
dc.author.googleKang, S-
dc.author.googleKim, DG-
dc.author.googleRhee, YH-
dc.relation.volume20-
dc.relation.issue49-
dc.relation.startpage16391-
dc.relation.lastpage16396-
dc.contributor.id10153778-
dc.relation.journalCHEMISTRY-A EUROPEAN JOURNAL-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationCHEMISTRY-A EUROPEAN JOURNAL, v.20, no.49, pp.16391 - 16396-
dc.identifier.wosid000345515700046-
dc.date.tcdate2019-01-01-
dc.citation.endPage16396-
dc.citation.number49-
dc.citation.startPage16391-
dc.citation.titleCHEMISTRY-A EUROPEAN JOURNAL-
dc.citation.volume20-
dc.contributor.affiliatedAuthorRhee, YH-
dc.identifier.scopusid2-s2.0-84915820662-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc3-
dc.description.scptc3*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusN-ACYLIMINIUM IONS-
dc.subject.keywordPlusOXOCARBENIUM IONS-
dc.subject.keywordPlusEFFICIENT SYNTHESIS-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusINDOLIZIDINES-
dc.subject.keywordPlusNUCLEOPHILES-
dc.subject.keywordPlusALLYLATION-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusAMINES-
dc.subject.keywordAuthordiastereoselectivity-
dc.subject.keywordAuthorenantioselectivity-
dc.subject.keywordAuthorheterocycles-
dc.subject.keywordAuthornatural products-
dc.subject.keywordAuthorsynthetic methods-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
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이영호RHEE, YOUNG HO
Dept of Chemistry
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