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

Giri, Awadut G. ; Mondal, Mohabul A. ; Puranik, Vedavati G. ; Ramana, Chepuri V. (2010) Effect of the allylic substituents on ring closing metathesis: The total synthesis of stagonolide B and 4-epi-stagonolide B Organic and Biomolecular Chemistry, 8 (2). pp. 398-406. ISSN 1477-0520

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Official URL: http://pubs.rsc.org/en/Content/ArticleLanding/2010...

Related URL: http://dx.doi.org/10.1039/B916198H

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.

Item Type:Article
Source:Copyright of this article belongs to Royal Society of Chemistry.
ID Code:106136
Deposited On:01 Feb 2018 16:54
Last Modified:01 Feb 2018 16:54

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