A rapid enantiospecific synthesis of the (6,6,5)-tricyclic ring system of the elisabethane diterpenes

Srikrishna, A and Pardeshi, Vijendra H and Satyanarayana, G (2007) A rapid enantiospecific synthesis of the (6,6,5)-tricyclic ring system of the elisabethane diterpenes. In: Tetrahedron Letters, 48 (23). pp. 4087-4090.

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Abstract

A rapid enantiospecific stereoselective synthesis of the 6,6,5-ring system of the novel tricyclic elisabethin diterpenes, starting from (R)-carvone, employing a ROM-RCM sequence as the key step, has been accomplished.

Item Type:	Journal Article
Publication:	Tetrahedron Letters
Publisher:	Elsevier
Additional Information:	Copyright of this article belongs to Elsevier.
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	03 Jul 2008
Last Modified:	19 Sep 2010 04:46
URI:	http://eprints.iisc.ac.in/id/eprint/14721

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