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

A rapid formal synthesis of the macrolide (-)-A26771B

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dc.contributor.authorLee, WWko
dc.contributor.authorShin, HJko
dc.contributor.authorChang, Sukbokko
dc.date.accessioned2013-03-04T11:15:06Z-
dc.date.available2013-03-04T11:15:06Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-02-
dc.identifier.citationTETRAHEDRON-ASYMMETRY, v.12, no.1, pp.29 - 31-
dc.identifier.issn0957-4166-
dc.identifier.urihttp://hdl.handle.net/10203/82464-
dc.description.abstract(-)-A26771B, a novel 16-membered macrolide with antibiotic activity, has been formally synthesized. In the synthesis ruthenium catalyzed ring-closing olefin metathesis (RCM) was used as a key reaction to construct the lactone ring. (C) 2001 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectEFFICIENT SYNTHESIS-
dc.subjectOLEFIN METATHESIS-
dc.subjectORGANIC-SYNTHESIS-
dc.subject(+)-ASPICILIN-
dc.subjectA26771B-
dc.subjectROUTE-
dc.titleA rapid formal synthesis of the macrolide (-)-A26771B-
dc.typeArticle-
dc.identifier.wosid000167494000003-
dc.identifier.scopusid2-s2.0-0035808908-
dc.type.rimsART-
dc.citation.volume12-
dc.citation.issue1-
dc.citation.beginningpage29-
dc.citation.endingpage31-
dc.citation.publicationnameTETRAHEDRON-ASYMMETRY-
dc.identifier.doi10.1016/S0957-4166(01)00004-0-
dc.contributor.localauthorChang, Sukbok-
dc.contributor.nonIdAuthorLee, WW-
dc.contributor.nonIdAuthorShin, HJ-
dc.type.journalArticleArticle-
dc.subject.keywordPlusEFFICIENT SYNTHESIS-
dc.subject.keywordPlusOLEFIN METATHESIS-
dc.subject.keywordPlusORGANIC-SYNTHESIS-
dc.subject.keywordPlus(+)-ASPICILIN-
dc.subject.keywordPlusA26771B-
dc.subject.keywordPlusROUTE-
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CH-Journal Papers(저널논문)
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