阿托品
化学
轴手性
催化作用
密度泛函理论
组合化学
钳子运动
位阻效应
手性(物理)
同种类的
计算化学
均相催化
有机化学
锰
立体化学
立体异构
化学选择性
对映选择合成
铑
立体选择性
生物催化
分子内力
产量(工程)
有机催化
反应条件
非共价相互作用
作者
Guanbo Li,Bo-Xuan Yao,Wen-Jing Yu,Xinru Chen,Xi Liu,Hengxian Mao,Shao‐Fei Ni,Weiping Liu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2026-02-24
卷期号:16 (5): 5218-5228
标识
DOI:10.1021/acscatal.6c00892
摘要
Homogeneous manganese pincer complexes have emerged as earth-abundant and versatile catalysts, offering a benign alternative to precious-metal-based systems in various organic transformations via metal–ligand cooperation (MLC). While these catalysts have demonstrated significant promise in asymmetric hydrogenation and the synthesis of central-chiral phosphines, their application in the construction of axial chirality remains largely underdeveloped. Herein, we report a manganese-catalyzed atroposelective hydrophosphination of sterically hindered 1-alkynylindoles with phosphines. This method provides a direct and efficient route to synthesize challenging C–N axially chiral vinylphosphine atropisomers with high regio- and enantioselectivity. The density functional theory (DFT) calculations demonstrated that the enantioselectivity is governed by the cooperative effect of multiple noncovalent interactions.
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