Tandem Cycloaddition Reactions of Allenyl Diazo Compounds Forming Triquinanes via Trimethylenemethane Diyls

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dc.contributor.authorKang, Taekko
dc.contributor.authorKim, Won-Yeobko
dc.contributor.authorYoon, Yeo-Kwonko
dc.contributor.authorKim, Byung-Gyuko
dc.contributor.authorLee, Hee-Yoonko
dc.date.accessioned2013-03-11T06:16:18Z-
dc.date.available2013-03-11T06:16:18Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2011-11-
dc.identifier.citationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.133, no.45, pp.18050 - 18053-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10203/98487-
dc.description.abstractA tandem reaction strategy for forming triquinanes from linear allenyl diazo compounds through an intramolecular 1,3-dipolar cycloaddition reaction of an allenyl diazo group that generates a trimethylenemethane (TMM) diyl followed by an intramolecular [2 + 3] TMM diyl cycloaddition reaction has been developed. The new tandem cycloaddition reaction is readily applicable to the synthesis of complex molecules with high versatility and efficiency.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectIDEAL SYNTHESIS-
dc.subjectCAPTURE-
dc.titleTandem Cycloaddition Reactions of Allenyl Diazo Compounds Forming Triquinanes via Trimethylenemethane Diyls-
dc.typeArticle-
dc.identifier.wosid000297381200013-
dc.identifier.scopusid2-s2.0-80755136888-
dc.type.rimsART-
dc.citation.volume133-
dc.citation.issue45-
dc.citation.beginningpage18050-
dc.citation.endingpage18053-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorLee, Hee-Yoon-
dc.type.journalArticleArticle-
dc.subject.keywordPlusIDEAL SYNTHESIS-
dc.subject.keywordPlusCAPTURE-
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