Prasad, KR and Gholap, SL (2005) An expeditious enantiospecific total synthesis of (+)-7-epi-goniofufurone. In: Synlett (14). pp. 2260-2262.
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Abstract
Stereoselective synthesis of styryl lactone, (+)-7-epi-goniofufurone was achieved in high yield via simple transformations from tartaric acid. The key step involves the successive stereoselective reduction of ketones with borohydride and selectride.
| Item Type: | Journal Article |
|---|---|
| Publication: | Synlett |
| Publisher: | Thieme Medical Publishers |
| Additional Information: | Copyright of this article belongs to Thieme Medical Publishers. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 08 Jun 2010 10:02 |
| Last Modified: | 08 Jun 2010 10:02 |
| URI: | http://eprints.iisc.ac.in/id/eprint/27195 |
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