Enantioselective method constructs chiral amines in ketones, highlighting a new synthetic approach.
Enantioselective α ‐amination of ketones represents a straightforward strategy for synthesizing highly valuable chiral α ‐amino ketones. However, most existing methods install a masked amino group, requiring additional steps to reveal the free amine. Consequently, the direct introduction of a simple alkylamino group at the ketone α ‐position remains underdeveloped. Herein, we report a dinickel‐catalyzed enantioselective α ‐amination of simple ketones that directly constructs chiral α ‐tertiary secondary amines. This reaction proceeds in moderate to good yield with good enantioselectivity via an S N 2 nucleophilic substitution at nitrogen by a dinickel enolate.
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Zhao et al. (2026) studied this question.
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