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An enantiospecific total synthesis of (-)-patchouli alcohol

Srikrishna, Adusumilli and Satyanarayana, Gedu (2005) An enantiospecific total synthesis of (-)-patchouli alcohol. In: Tetrahedron: Asymmetry, 16 (24). pp. 3992-3997.

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An enantiospecific total synthesis of patchouli alcohol, starting from the readily available monoterpene (R)-carvone, has been accomplished. A tandem double Michael reaction-alkylation sequence and single electron mediated 6-endo trig cyclisation reaction have been employed as key steps.

Item Type: Journal Article
Additional Information: Copyright for this article belongs to Elsevier Ltd.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Depositing User: B.S Priyanka
Date Deposited: 26 Nov 2007
Last Modified: 19 Sep 2010 04:23
URI: http://eprints.iisc.ac.in/id/eprint/5165

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