对映选择合成
化学
产量(工程)
酮
群(周期表)
亲核细胞
亲核取代
立体化学
有机化学
保护组
手性助剂
氮气
催化作用
组合化学
立体异构
简单(哲学)
氨基酸
亲核加成
对映体过量
反应条件
功能群
正在离开组
作者
Yuchi Zhao,Yanxin Gu,Li Li,Zhonglin Tao
摘要
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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