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dc.contributor.authorSrikrishna, A-
dc.contributor.authorRao, M Sreenivasa-
dc.date.accessioned2008-04-02T11:21:37Z-
dc.date.available2008-04-02T11:21:37Z-
dc.date.issued2007-08-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/673-
dc.description1308-1317en_US
dc.description.abstractA sequence comprising of Johnson's ortho ester Claisen rearrangement, alkylation and RCM reactions has been developed for the synthesis of cyclopentenes containing vicinal quaternary carbon atoms. The versatility of the sequence has been demonstrated by the efficient total synthesis of sesquiterpenes tochuinyl acetates and herbertene-1,14-diol.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.46B(8) [August 2007]en_US
dc.subjectTerpene synthesisen_US
dc.subjectVicinal quaternary carbonsen_US
dc.subjectClaisen rearrangementen_US
dc.subjectRing-closing metathesisen_US
dc.subjectHerbertanesen_US
dc.subjectCuparanesen_US
dc.titleAn RCM based approach to (±)-herbertene-1, 14-diol and (±)-tochuinyl acetatesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.46B(08) [August 2007]

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