Stereoselectivity in Trimethylenemethane (TMM) Diyl Mediated Cycloaddition Reaction to Angularly Fused Triquinanes

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dc.contributor.authorYoon, Yeo-Kwonko
dc.contributor.authorKang, Taekko
dc.contributor.authorLee, Hee-Yoonko
dc.date.accessioned2013-03-11T06:16:48Z-
dc.date.available2013-03-11T06:16:48Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2011-02-
dc.identifier.citationCHEMISTRY-AN ASIAN JOURNAL, v.6, no.2, pp.646 - 651-
dc.identifier.issn1861-4728-
dc.identifier.urihttp://hdl.handle.net/10203/98488-
dc.description.abstractA thorough study on the diastereoselectivity in the TMM diyl mediated [2+3] cycloaddition reaction of monosubstituted linear substrates to form angularly fused triquinanes was carried out. Substitution at position 3 provided complete diastereoselectivity, while positions 1 and 4 induced marginal stereoselectivity. Position 2 did not show any influence on the diastereoselectivity. Position 4 turned out to be incompatible with the cycloaddition reaction as the carbene intermediate underwent O-Si bond insertion to form a dihydrofuran ring.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectKETONES-
dc.titleStereoselectivity in Trimethylenemethane (TMM) Diyl Mediated Cycloaddition Reaction to Angularly Fused Triquinanes-
dc.typeArticle-
dc.identifier.wosid000286440600051-
dc.identifier.scopusid2-s2.0-79251518940-
dc.type.rimsART-
dc.citation.volume6-
dc.citation.issue2-
dc.citation.beginningpage646-
dc.citation.endingpage651-
dc.citation.publicationnameCHEMISTRY-AN ASIAN JOURNAL-
dc.identifier.doi10.1002/asia.201000672-
dc.contributor.localauthorLee, Hee-Yoon-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcarbenes-
dc.subject.keywordAuthorcycloaddition-
dc.subject.keywordAuthorstereoselectivity-
dc.subject.keywordAuthortrimethylenemethane-
dc.subject.keywordAuthortriquinane-
dc.subject.keywordPlusKETONES-
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