Total synthesis of enokipodins A-D and cuparene-1,4-diol

Srikrishna, A and Rao, Srinivasa M (2010) Total synthesis of enokipodins A-D and cuparene-1,4-diol. In: Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry, 49 (10). pp. 1363-1371.

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Abstract

A Claisen rearrangement and RCM reaction based sequence has been developed for total synthesis of the antifungal sesquiterpenes enokipodins A-D and cuparene-1,4-diol starting from 2,5-dimethoxy-4-methylhydroquinone.

Item Type:	Journal Article
Publication:	Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry
Publisher:	National Institute of Science Communication and Information Resources.
Additional Information:	Copyright of this article belongs to National Institute of Science Communication and Information Resources.
Keywords:	Enokipodins; cuparenes; RCM reaction; Claisen rearrangement; sesquiterpenes
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	18 Nov 2010 12:22
Last Modified:	18 Nov 2010 12:22
URI:	http://eprints.iisc.ac.in/id/eprint/33842

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