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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Abstract

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
Publication:	Tetrahedron: Asymmetry
Publisher:	Elsevier Ltd
Additional Information:	Copyright for this article belongs to Elsevier Ltd.
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
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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