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A Nucleophilic Strategy for Enantioselective Intermolecular α‑Amination: Access to Enantioenriched α‑Arylamino Ketones

Published Web Location

https://doi.org/10.1021/jacs.5b04518
Abstract

The enantioselective addition of anilines to azoalkenes was accomplished through the use of a chiral phosphoric acid catalyst. The resulting α-arylamino hydrazones were obtained in good yields and excellent enantioselectivities and provide access to enantioenriched α-arylamino ketones. A serendipitous kinetic resolution of racemic α-arylamino hydrazones is also described.

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