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College of Natural Sciences(자연과학대학)Dept. of Chemistry(화학과)CH-Journal Papers(저널논문)

An asymmetric aminohydroxylation approach to the stereoselective synthesis of cis-substituted azetidinone of loracarbef

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dc.contributor.authorLee, JCko
dc.contributor.authorKim, GTko
dc.contributor.authorShim, YKko
dc.contributor.authorKang, SungHoko
dc.date.accessioned2013-03-04T17:44:18Z-
dc.date.available2013-03-04T17:44:18Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-07-
dc.identifier.citationTETRAHEDRON LETTERS, v.42, no.27, pp.4519 - 4521-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/83499-
dc.description.abstractA formal synthesis of loracarbef is described. The required key cia-substituted azetidinone skeleton was stereoselectively constructed via p-amino acid, which was provided from the asymmetric aminohydroxylation of alpha,beta -unsaturated ester. (C) 2001 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectCARBACEPHEM FRAMEWORK-
dc.subjectAMINO ACIDS-
dc.titleAn asymmetric aminohydroxylation approach to the stereoselective synthesis of cis-substituted azetidinone of loracarbef-
dc.typeArticle-
dc.identifier.wosid000169398900025-
dc.identifier.scopusid2-s2.0-0035797052-
dc.type.rimsART-
dc.citation.volume42-
dc.citation.issue27-
dc.citation.beginningpage4519-
dc.citation.endingpage4521-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorLee, JC-
dc.contributor.nonIdAuthorKim, GT-
dc.contributor.nonIdAuthorShim, YK-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorasymmetric aminohydroxylation-
dc.subject.keywordAuthorloracarbef-
dc.subject.keywordAuthorcarbacephalosporin-
dc.subject.keywordAuthorcis-azetidinone-
dc.subject.keywordPlusCARBACEPHEM FRAMEWORK-
dc.subject.keywordPlusAMINO ACIDS-
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CH-Journal Papers(저널논문)
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