451-40-1 Highly regioselective copper-catalyzed benzylic C-H amination by N-fluorobenzenesulfonimide

Primary target: A practical and effective copper-catalyzed amination strategy for synthesizing various benzylic amines from benzylic hydrocarbons is described (see scheme; DCE=1,2-dichloroethane). Xylene substrates can undergo diamination reactions using this method. The remarkable preference for primary over secondary benzylic C-H bonds has been observed for the first time. Copyright https://www.lookchem.com/CASDataBase_451-40-1.htm

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