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A process for the rapid removal of dialkylamino-substituents from aromatic rings. Application to the expedient synthesis of (R)-tolterodine
Authors:Nick A Paras
Institution:Merck Center for Catalysis, Princeton University, Princeton, NJ 08544, United States
Abstract:A range of N,N-dialkylanilines have been successfully converted to the parent substituted benzenes by a novel two-step pathway. The products are obtained in good yields and optical purity of adjacent stereocenters is maintained. This technology has been applied toward the synthesis of (R)-tolterodine.
Keywords:Reductive deamination  Organocatalysis  Enantioselective  Tolterodine
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