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An efficient approach for the total synthesis of balticolid
Authors:DGS Sudhakar  Ch Venkata Ramana Reddy  Srinivasa Rao Alapati
Institution:1. GVK Biosciences Private Limited, Medicinal Chemistry Division 28A, IDA, Nacharam, Hyderabad 500076, Telangana, India;2. Department of Chemistry, Jawaharlal Nehru Technological University, Hyderabad 500 085, Telangana, India
Abstract:An efficient stereoselective total synthesis of balticolid has been accomplished starting from known aldehyde. The key steps involved in this synthesis are Sharpless asymmetric epoxidation, Wittig olefination, alkylation of 1,3-dithiane and Yamaguchi macrolactonization.
Keywords:Corresponding author    12-Membered macrolides  Sharpless asymmetric epoxidation  Wittig olefination  Yamaguchi macrolactonization
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