Total Synthesis of (-)-13-Acetoxymodhephene and (+)-14-Acetoxymodhephene

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dc.contributor.authorMurugan, RNko
dc.contributor.authorLee, Hee Yoonko
dc.contributor.authorMurugan, RNko
dc.contributor.authorMoon, Deuk Kyuko
dc.date.accessioned2013-03-08T19:01:26Z-
dc.date.available2013-03-08T19:01:26Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2009-10-
dc.identifier.citationEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, no.29, pp.5028 - 5037-
dc.identifier.issn1434-193X-
dc.identifier.urihttp://hdl.handle.net/10203/93980-
dc.description.abstractStereoselective epoxidation of [4.3.3]propellane 16 set the stage for the Lewis acid catalyzed stereospecific ring contraction to an oxygenated modhephene structure and eventually led to the total synthesis of (-)-13-acetoxymodhephene and (+)-14-acetoxyrnodhephene. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectENANTIOSELECTIVE SYNTHESIS-
dc.subjectABSOLUTE-CONFIGURATION-
dc.subjectOPTICAL RESOLUTION-
dc.subjectMODHEPHENE-
dc.subjectSESQUITERPENES-
dc.subjectALCOHOLS-
dc.subjectREAGENT-
dc.subjectKETONES-
dc.subject(+/-)-MODHEPHENE-
dc.subject(-)-MODHEPHENE-
dc.titleTotal Synthesis of (-)-13-Acetoxymodhephene and (+)-14-Acetoxymodhephene-
dc.typeArticle-
dc.identifier.wosid000271010600015-
dc.type.rimsART-
dc.citation.issue29-
dc.citation.beginningpage5028-
dc.citation.endingpage5037-
dc.citation.publicationnameEUROPEAN JOURNAL OF ORGANIC CHEMISTRY-
dc.identifier.doi10.1002/ejoc.200900713-
dc.contributor.localauthorLee, Hee Yoon-
dc.contributor.nonIdAuthorMurugan, RN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusABSOLUTE-CONFIGURATION-
dc.subject.keywordPlusOPTICAL RESOLUTION-
dc.subject.keywordPlusMODHEPHENE-
dc.subject.keywordPlusSESQUITERPENES-
dc.subject.keywordPlusALCOHOLS-
dc.subject.keywordPlusREAGENT-
dc.subject.keywordPlusKETONES-
dc.subject.keywordPlus(+/-)-MODHEPHENE-
dc.subject.keywordPlus(-)-MODHEPHENE-
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