Total Synthesis of (-)-Crinipellin A

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dc.contributor.authorKang, Taekko
dc.contributor.authorSong, Seog Beomko
dc.contributor.authorKim, Won Yeobko
dc.contributor.authorKim, Byung Gyuko
dc.contributor.authorLee, Hee Yoonko
dc.date.accessioned2014-12-09T01:24:27Z-
dc.date.available2014-12-09T01:24:27Z-
dc.date.created2014-09-02-
dc.date.created2014-09-02-
dc.date.created2014-09-02-
dc.date.issued2014-07-
dc.identifier.citationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.136, no.29, pp.10274 - 10276-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10203/192380-
dc.description.abstractThe first total synthesis of (-)-crinipellin A is described. The tetraquinane core skeleton of crinipellin A was assembled through the tandem [2 + 3] cycloaddition reaction of an allenyl diazo substrate containing a cyclopentane ring in a single operation. The absolute stereochemistry was confirmed through the total synthesis.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleTotal Synthesis of (-)-Crinipellin A-
dc.typeArticle-
dc.identifier.wosid000339471900024-
dc.identifier.scopusid2-s2.0-84904865658-
dc.type.rimsART-
dc.citation.volume136-
dc.citation.issue29-
dc.citation.beginningpage10274-
dc.citation.endingpage10276-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.identifier.doi10.1021/ja5054412-
dc.contributor.localauthorLee, Hee Yoon-
dc.contributor.nonIdAuthorKim, Byung Gyu-
dc.type.journalArticleArticle-
dc.subject.keywordPlus1,3-DIYL TRAPPING REACTION-
dc.subject.keywordPlusTRIMETHYLENEMETHANE DIYLS-
dc.subject.keywordPlusCYCLOADDITION REACTIONS-
dc.subject.keywordPlusASYMMETRIC INDUCTION-
dc.subject.keywordPlusCARBONYL-COMPOUNDS-
dc.subject.keywordPlusDIAZO-COMPOUNDS-
dc.subject.keywordPlusIDEAL SYNTHESIS-
dc.subject.keywordPlusCRINIPELLIN B-
dc.subject.keywordPlusTRIQUINANES-
dc.subject.keywordPlusOXIDATION-
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