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Stereoselective total synthesis of sporiolide B and attempted synthesis of sporiolide A
Authors:Gattu Sridhar  Gangavaram V M Sharma
Institution:1. Organic and Biomolecular Chemistry Division, CSIR Indian Institute of Chemical Technology, Hyderabad, Indiasridhar1org@yahoo.com;3. Organic and Biomolecular Chemistry Division, CSIR Indian Institute of Chemical Technology, Hyderabad, India
Abstract:A simple and efficient stereoselective total synthesis of sporiolide B and attempted synthesis of sporiolide A, from epichlorohydrin, using asymmetric synthetic approach is reported. The key reactions involved are Sharpless epoxidation, Jacobsen reaction, syn-allylation, Yamaguchi esterification, and Grubbs ring-closing metatheses reaction to result in the macrocyclic ring system.
Keywords:Ring-closing metathesis  syn-allylation  sporiolide A  sporiolide B  Yamaguchi esterification
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