对映选择合成
立体中心
废止
催化作用
化学
组合化学
立体化学
有机化学
作者
Lin Ye,Tristan von Münchow,Lutz Ackermann
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2023-07-11
卷期号:13 (14): 9713-9723
被引量:59
标识
DOI:10.1021/acscatal.3c02072
摘要
The 3d metallaelectro-catalyzed C-H activation has been identified as an increasingly viable strategy to access valuable organic molecules in a resource-economic fashion under exceedingly mild reaction conditions. However, the development of enantioselective 3d metallaelectro-catalyzed C-H activation is very challenging and in its infancy. Here, we disclose the merger of cobaltaelectro-catalyzed C-H activation with asymmetric catalysis for the highly enantioselective annulation of allenes. A broad range of C-N axially chiral and P-stereogenic compounds were thereby obtained in good yields of up to 98% with high enantioselectivities of up to >99% ee. The practicality of this approach was demonstrated by the diversification of complex bioactive compounds and drug molecules as well as decagram scale enantioselective electrocatalysis in continuous flow.
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