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Abstract
The enantio- and regioselective reductive hydroarylation
of N-acyl enamines has been achieved with a NiH catalyst and a
chiral bis-imidazoline ligand. A broad range of structurally diverse,
enantioenriched benzylamines, a moiety found in many
pharmacologically active molecules, have been synthesized
efficiently under mild, operationally simple reaction conditions.
Supplementary materials
Title
Asymmetric Hydroarylation of N-Acyl Enamine SI
Description
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