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The First Total Synthesis of the Antimicrobial Sesquiterpenes (±)-Enokipodins A and B

Srikrishna, A and Rao, Srinivasa M (2004) The First Total Synthesis of the Antimicrobial Sesquiterpenes (±)-Enokipodins A and B. In: Synlett, 2 . pp. 374-376.

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Abstract

Efficient first total synthesis of antimicrobial sesquiterpenes enokipodins A and B (1 and 2, respectively) and formal total synthesis of cuparene-1,4-diol (5) and cuparene-1,4-quinone (7) have been accomplished starting from 2,5-dimethoxy-4-methylacetophenone employing Claisen rearrangement and ring-closing metathesis reaction as key steps.

Item Type: Journal Article
Additional Information: The copyright belongs to Thieme.
Keywords: Sesquiterpenes;enokipodins A and B;Ring;Cosing metathesis;Claisen rearrangement
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 27 May 2006
Last Modified: 27 Aug 2008 12:03
URI: http://eprints.iisc.ernet.in/id/eprint/6984

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