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Stereoselective synthesis of the C3-C15 fragment of callyspongiolide
Authors:Gopal Reddy Ramidi  Jhillu S Yadav  Debendra K Mohapatra
Institution:1. Organic Synthesis and Process Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India;2. Academy of Scientific and Innovative Research (AcSIR), Mathura Road, New Delhi 110 025, India;3. School of Science, Indrashil University, Kadi, Gujarat 382740, India
Abstract:The synthesis of C3-C15 fragment of callyspongiolide, a 14-membered macrolides isolated from the marine sponge Callyspongia sp., which was collected from the Indonesia, is reported. Highlights of the synthesis include construction of E-olefin through Julia-Kocienski olefination, Brown asymmetric allylation and base-induced elimination reactions for propargyl alcohol synthesis.
Keywords:Callyspongiolide  Natural products  Julia-Kocienski olefination  Brown asymmetric allylation  Base-induced elimination reaction
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