A stereoselective approach for the total synthesis of clonostachydiol

Yadav, J. S. ; Swamy, T. ; Subba Reddy, B. V. (2008) A stereoselective approach for the total synthesis of clonostachydiol Synlett, 2008 (18). pp. 2773-2776. ISSN 0936-5214

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Official URL: http://www.thieme-connect.com/ejournals/abstract/s...

Related URL: http://dx.doi.org/10.1055/s-0028-1087296

Abstract

A stereoselective synthesis of clonostachydiol is accomplished using readily available (±)-epichlorohydrin as a precursor. The synthesis involves direct and straightforward reactions such as Sharpless asymmetric epoxidation, iodination, stereoselective opening of epoxide with allylmagnesium chloride and Sharpless asymmetric dihydroxylation.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Sharpless Asymmetric Epoxidation; Allylmagnesium Chloride; Sharpless Asymmetric Dihydroxylation
ID Code:63106
Deposited On:28 Sep 2011 03:37
Last Modified:28 Sep 2011 03:37

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