Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21635
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dc.contributor.authorSrikrishna, A-
dc.contributor.authorBabu, N Chandrasekhar-
dc.contributor.authorDethe, Dattatraya H-
dc.date.accessioned2013-10-07T10:03:13Z-
dc.date.available2013-10-07T10:03:13Z-
dc.date.issued2003-07-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21635-
dc.description1688-1690en_US
dc.description.abstractAn enantiospecific formal total synthesis of (-)-ceratopicanol starting from the readily and abundantly available monoterpene (R)-limonene is described. A combination of Claisen rearrangement- intramolecular diazo ketone cyclopropanation-regiospecific reductive cyclopropane cleavage reactions are employed for the stereo- and regiospecific generation of the two vicinal ring junction quaternary carbon atoms.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(07) [July 2003]en_US
dc.titleA convenient enantiospecific methodology for (-)-(1R,5S)-1 ,5-dimethylbicyclo[3.3.0]octa-2,7-dione: A formal total synthesis of (-)-ceratopicanolen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(07) [July 2003]

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