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dc.contributor.authorSrikrishna, A-
dc.contributor.authorReddy, T Jagadeeswara-
dc.contributor.authorKumar, P Praveen-
dc.date.accessioned2008-04-03T10:29:12Z-
dc.date.available2008-04-03T10:29:12Z-
dc.date.issued2007-09-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/700-
dc.description1518-1525en_US
dc.description.abstractAn intramolecular alkylation based approach has been explored for the enantiospecific construction of AB-ring system of taxanes starting from 3-allyl-4,4-dimethylcarvone, which however led only to bicyclo[2.2.2]octanones.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.46B(9) [September 2007]en_US
dc.subjectTaxanesen_US
dc.subjectIntramolecular alkylationen_US
dc.subjectBicyclo[5.3.1]undecanesen_US
dc.subjectCarvoneen_US
dc.subjectBicyclo[2.2.2]octanesen_US
dc.titleExploratory studies towards AB-ring system of taxanes via intramolecular alkylation reaction. Formation of bicyclo[2.2.2]octanones in preference to bicyclo[5.3.1]undecanesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.46B(09) [September 2007]

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