Prasad, Kavirayani R and Kumar, Mothish S (2011) Total Synthesis of Gabosine H. In: Synlett (11). pp. 1602-1604.
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Official URL: https://www.thieme-connect.de/DOI/DOI?10.1055/s-00...
Abstract
Stereoselective total synthesis and assignment of the absolute configuration of the keto carba sugar gabosine H is presented. Pivotal reactions in the sequence include desymmetrization of the dimethylamide of tartaric acid and ring-closing metathesis.
| Item Type: | Journal Article |
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| Additional Information: | Copyright of this article belongs to Thieme Medical Publishers. |
| Keywords: | gabosine H;natural products;stereoselective synthesis; ring-closing metathesis |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 05 Jul 2011 10:09 |
| Last Modified: | 05 Jul 2011 10:09 |
| URI: | http://eprints.iisc.ernet.in/id/eprint/38870 |
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