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dc.contributor.authorSrikrishna, A-
dc.contributor.authorKumar, P Ravi-
dc.date.accessioned2008-09-15T10:13:28Z-
dc.date.available2008-09-15T10:13:28Z-
dc.date.issued2008-09-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/2003-
dc.description1414-1422en_US
dc.description.abstractEnantiospecific synthesis of (+)-trans-⍺-himachalene starting from (R)-carvone is described. An intramolecular type II carbonyl ene reaction has been employed as the key step for the construction of the bicyclo[5.4.0]undecane ring system.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.47B(9) [Sepetember 2008]en_US
dc.subjectEnantiospecific synthesisen_US
dc.subjectHimachalenesen_US
dc.subjectSesquiterpenesen_US
dc.subject(R)-carvoneen_US
dc.subjectIntramolecular ene-reactionen_US
dc.titleEnantiospecific synthesis of (+)-trans-⍺-himachalene via an intramolecular type II carbonyl ene reactionen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.47B(09) [September 2008]

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