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Stereoselective total synthesis of stagonolide E
Authors:Gowravaram Sabitha  P. Padmaja  P. Narayana Reddy  Surender Singh Jadav  J.S. Yadav
Affiliation:Organic Division I, Indian Institute of Chemical Technology, Hyderabad 500 607, India
Abstract:The first total synthesis of a 10-membered macrolide, stagonolide E is described from readily available 4-penten-1-ol. The synthetic strategy involves Jacobsen’s kinetic resolution, Sharpless epoxidation, Stille-Gennari, and Yamaguchi lactonization as key reactions.
Keywords:Macrolide   Jacobsen&rsquo  s kinetic resolution   Sharpless epoxidation   Stille-Gennari   Yamaguchi lactonization
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