Issue 2, 2010

Effect of the allylic substituents on ring closing metathesis: the total synthesis of stagonolide B and 4-epi-stagonolide B

Abstract

The total syntheses of stagonolide B and its 4-epimer were carried out to probe into how the relative stereochemistry of allylic hydroxy groups and their protecting groups influence the efficiency of the ring closing metathesis.

Graphical abstract: Effect of the allylic substituents on ring closing metathesis: the total synthesis of stagonolide B and 4-epi-stagonolide B

Supplementary files

Article information

Article type
Paper
Submitted
06 Aug 2009
Accepted
29 Sep 2009
First published
29 Oct 2009

Org. Biomol. Chem., 2010,8, 398-406

Effect of the allylic substituents on ring closing metathesis: the total synthesis of stagonolide B and 4-epi-stagonolide B

A. G. Giri, M. A. Mondal, V. G. Puranik and C. V. Ramana, Org. Biomol. Chem., 2010, 8, 398 DOI: 10.1039/B916198H

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