A process for the rapid removal of dialkylamino-substituents from aromatic rings. Application to the expedient synthesis of (R)-tolterodine |
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Authors: | Nick A. Paras |
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Affiliation: | Merck Center for Catalysis, Princeton University, Princeton, NJ 08544, United States |
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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. |
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Keywords: | Reductive deamination Organocatalysis Enantioselective Tolterodine |
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