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Total synthesis of mangiferaelactone
Authors:Paresh M Vadhadiya  CV Ramana
Institution:Division of Organic Chemistry, CSIR-National Chemical Laboratory, Pune 411 008, India
Abstract:Herein we document the first total synthesis of mangiferaelactone and thus establish its absolute configuration. The central nonenolide ring was constructed using ring closing metathesis and Yamaguchi esterification. The key alcohol fragment was synthesized by the Bernet–Vasella fragmentation of C-ribofuranoside.
Keywords:Total synthesis  Nonenolide  Ring closing metathesis  Bernet&ndash  Vasella fragmentation  Yamaguchi protocol
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