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Highly Regioselective Ring Opening of Epoxides with Thiols Catalyzed by SbCl3 Under Solvent-Free Conditions
Authors:Dadkhoda Ghazanfari  Mohammed M Hashemi  Mohammad Reza Akhgar  Mohammad Mehdi Foroughi  Fariba Najafi-Zadeh
Institution:1. Department of Chemistry , Islamic Azad University , Kerman Branch, Kerman, Iran;2. Department of Chemistry , Sharif University of Technology , Tehran, Iran
Abstract:The ring-opening reaction of epoxides with thiols by SbCl 3 supported on Kieselguhr under solvent-free conditions, afforded high yields of β-hydroxy sulfides. Nucleophilic attack of the thiols occurs regioselectively at the less hindered side of the epoxides.
Keywords:β-hydroxysulfides  epoxides  ring opening  SbCl3  solvent-free reaction  thiols
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