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Stereoselective Total Synthesis of Stagonolide C
Authors:Jhillu S. Yadav  Nimmakayala Mallikarjuna Reddy  N. Venkateswar Rao  Md. Ataur Rahman  Attaluri R. Prasad
Affiliation:1. Organic Division‐I, Indian Institute of Chemical Technology, Hyderabad‐500007, India, (fax: +91‐40‐27160512);2. King Saud University, Riyadh‐11451, Saudi Arabia
Abstract:A convergent and efficient total synthesis of stagonolide C ( 1 ), a phytotoxic metabolite, was achieved (Schemes 2 and 3) The synthesis exploited the high configuration control in the Prins cyclization along with alkene rearrangement and ring‐closing metathesis as key steps.
Keywords:Stagonolide C  Prins cyclization  Alkene rearrangement  Ring‐closing metathesis
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