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Radical trifluoromethylation of ketone silyl enol ethers by activation with dialkylzinc
Authors:Mikami Koichi  Tomita Yuichi  Ichikawa Yoshiyuki  Amikura Kazutoshi  Itoh Yoshimitsu
Institution:Department of Applied Chemistry, Tokyo Institute of Technology, Tokyo 152-8552, Japan. kmikami@o.cc.titech.ac.jp
Abstract:reaction: see text] The radical trifluoromethylation of ketone silyl enol ethers gave alpha-CF(3) ketones in good yields with wide scope of the ketonic substrates including acyclic ketones and cyclopentanone. The use of dialkylzinc to activate the silyl enol ethers is the key to the efficient radical trifluoromethylation.
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