Asymmetric Synthesis of α-Amino Ketones by Brønsted Acid Catalysis

Brønsted–Lowry acid–base theory Reductive amination Transfer hydrogenation
DOI: 10.1021/acs.orglett.5b01972 Publication Date: 2015-07-28T13:34:38Z
ABSTRACT
The highly efficient, regioselective, and enantioselective transfer hydrogenation of α-keto ketimines reductive amination diketones by Brønsted acid catalysis is described. A series chiral α-amino ketones prepared in high yields (up to >99%), excellent regioselectivities >99:1), enantioselectivities 98% ee). This method has broad substrate scope.
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