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dc.contributor.authorSrikrishna, A-
dc.contributor.authorKumar, P Praveen-
dc.contributor.authorReddy, T Jagadeeswar-
dc.date.accessioned2010-05-31T10:40:15Z-
dc.date.available2010-05-31T10:40:15Z-
dc.date.issued2005-07-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9149-
dc.description1430-1436en_US
dc.description.abstractEnantiospecific syntheses of B-seco­-nortaxanes have been accomplished starting from the readily and abundantly available monoterperpene (R)-carvone. Carvone has been converted into both A-ring as well as C-ring derivatives of taxane and coupled with a two carbon unit.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Cen_US
dc.sourceIJC-B Vol.44B(07) [July 2005]en_US
dc.subjectEnantiospecific synthesesen_US
dc.subjectseco-nortaxanesen_US
dc.subjectcarvoneen_US
dc.subjectmonoterpeneen_US
dc.titleEnantiospecific synthesis of B-seco-nortaxanes from two molecules of carvoneen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(07) [July 2005]

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