A concise approach for the synthesis of core fragment C7-C15 of (+)-migrastatin using desymmetrization strategy

Yadav, J. S. ; Naga Lakshmi, P. (2010) A concise approach for the synthesis of core fragment C7-C15 of (+)-migrastatin using desymmetrization strategy Synlett, 2010 (7). pp. 1033-1036. ISSN 0936-5214

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

Related URL: http://dx.doi.org/10.1055/s-0029-1219785

Abstract

The core fragment C7-C15 the (+)-migrastatin was constructed in a stereoconvergent manner utilizing desymmetrization approach. The strategy involved the generation of Z-configuration of trisubstituted double bond at C11-C12, epimerization at C10, ring opening of the pyran lactol with C2 Wittig ylide, and regioselective Sharpless dihydroxylation.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:(+)-migrastatin; Desymmetrization; Epimerization; Sharpless Asymmetric Dihydroxylation
ID Code:63157
Deposited On:28 Sep 2011 03:45
Last Modified:28 Sep 2011 03:45

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