Total Synthesis of Gabosine H

Prasad, Kavirayani R and Kumar, Mothish S (2011) Total Synthesis of Gabosine H. In: Synlett (11). pp. 1602-1604.

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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
Publication:	Synlett
Publisher:	Thieme Medical Publishers
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.ac.in/id/eprint/38870

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