Towards a Practical Br�nsted Acid Catalyzed and Hantzsch Ester Mediated Asymmetric Reductive Amination of Ketones with Benzylamine.

We report the use of benzylamine as the amine component in Hantzsch ester mediated and chiral Br�nsted acid catalyzed enantioselective reductive aminations of ketones. The method is noteworthy because the benzyl group is easily removable, and amine product purification is achieved through Hantzsch ester oxidation product removal via basic hydrolysis. [ABSTRACT FROM AUTHOR]