Prasad, Kavirayani R and Anbarasan, Pazhamalai (2007) Enantiodivergent Synthesis of Both Enantiomers of Gypsy Moth Pheromone Disparlure. In: Journal of Organic Chemistry, 72 (8). pp. 3155-3157.
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Abstract
Enantiodivergent synthesis of both (-)- and (+)-disparlure, a bioactive pheromone, possessing a cis-epoxide has been accomplished. The key step involves the cross metathesis of a chiral homoallylic alcohol derived from L-(+)-tartaric acid.
Item Type: | Journal Article |
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Publication: | Journal of Organic Chemistry |
Publisher: | American Chemical Society |
Additional Information: | Copyright of this article belongs to American Chemical Society. |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 25 Jul 2008 |
Last Modified: | 19 Sep 2010 04:48 |
URI: | http://eprints.iisc.ac.in/id/eprint/15263 |
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