Prasad, Kavirayani R. ; Anbarasan, Pazhamalai (2007) Enantiodivergent synthesis of both enantiomers of gypsy moth pheromone disparlure The Journal of Organic Chemistry, 72 (8). pp. 3155-3157. ISSN 0022-3263
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Official URL: http://pubs.acs.org/doi/abs/10.1021/jo070060o
Related URL: http://dx.doi.org/10.1021/jo070060o
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: | Article |
|---|---|
| Source: | Copyright of this article belongs to American Chemical Society. |
| ID Code: | 105834 |
| Deposited On: | 21 Dec 2017 12:02 |
| Last Modified: | 21 Dec 2017 12:02 |
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