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An expeditious enantiospecific total synthesis of (+)-7-epi-goniofufurone

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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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
Additional Information: Copyright of this article belongs to Thieme Medical Publishers.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Depositing User: Ms G Yashodha
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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