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

Concise Total Synthesis and Stereochemical Revision of all (-)-Trigonoliimines

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dc.contributor.authorHan, Sunkyuko
dc.contributor.authorMovassaghi, Mohammadko
dc.date.accessioned2015-11-20T10:25:05Z-
dc.date.available2015-11-20T10:25:05Z-
dc.date.created2014-07-07-
dc.date.created2014-07-07-
dc.date.created2014-07-07-
dc.date.issued2011-07-
dc.identifier.citationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.133, no.28, pp.10768 - 10771-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10203/201398-
dc.description.abstractThe concise and enantioselective total syntheses of (-)-trigonoliimines A, B, and C are described. Our unified strategy to all three natural products is based on asymmetric oxidation and reorganization of a single bistryptamine, a sequence of transformations with possible biogenetic relevance. We revise the absolute stereo chemistry of (-)-trigonoliimines A, B, and C.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleConcise Total Synthesis and Stereochemical Revision of all (-)-Trigonoliimines-
dc.typeArticle-
dc.identifier.wosid000293113200024-
dc.identifier.scopusid2-s2.0-79960209676-
dc.type.rimsART-
dc.citation.volume133-
dc.citation.issue28-
dc.citation.beginningpage10768-
dc.citation.endingpage10771-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.identifier.doi10.1021/ja204597k-
dc.contributor.localauthorHan, Sunkyu-
dc.contributor.nonIdAuthorMovassaghi, Mohammad-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusSTEREOCONTROLLED TOTAL-SYNTHESIS-
dc.subject.keywordPlusASYMMETRIC EPOXIDATION-
dc.subject.keywordPlusENANTIOSELECTIVE EPOXIDATION-
dc.subject.keywordPlusOXIDATIVE REARRANGEMENT-
dc.subject.keywordPlusROOM-TEMPERATURE-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusOLEFINS-
dc.subject.keywordPlusBIOSYNTHESIS-
dc.subject.keywordPlusDERIVATIVES-
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CH-Journal Papers(저널논문)
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