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 |
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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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