Prasad, Kavirayani R. ; Anbarasan, Pazhamalai (2006) Enantiospecific synthesis of (−)-muricatacin from L-(+)-tartaric acid Tetrahedron: Asymmetry, 17 (17). pp. 2465-2467. ISSN 0957-4166
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetasy.2006.09.017
Abstract
Enantiospecific synthesis of (−)-muricatacin, a bio-active lactone comprising of a 5-hydroxyalkylbutan-4-olide structural component has been achieved from L-(+)-tartaric acid. The key step involves a disteroselective reduction of a C2-symmetric 1,4-diketone derived from tartaric acid followed by a selective Grignard reagent addition.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 105838 |
| Deposited On: | 21 Dec 2017 12:04 |
| Last Modified: | 21 Dec 2017 12:04 |
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