化学
动力学分辨率
亲核细胞
催化作用
激进的
电泳剂
催化循环
配体(生物化学)
试剂
对映选择合成
组合化学
不对称诱导
立体化学
计算化学
有机化学
生物化学
受体
作者
Kaidi Li,Baptiste Leforestier,Amalia I. Poblador‐Bahamonde,Céline Besnard,Laure Guénée,Svetlana Kucher,Clément Mazet
标识
DOI:10.1021/acscatal.4c06360
摘要
A Ni-catalyzed enantioconvergent cross-coupling between β-bromostyrenes and secondary Grignard reagents is reported. This C(sp2)–C(sp3) cross-coupling is applicable to a broad range of electrophilic and nucleophilic partners and affords the products in good to high levels of enantio-induction. Experimental mechanistic investigations revealed an unexpected binding mode of the chiral (P,N) ligand and support a radical rebound mechanism involving in-cage radicals. Kinetic experiments provide evidence for an off-cycle resting state featuring dinuclear species. Computational analyses are in line with this hypothesis and coherent with a catalytic cycle proceeding via a Ni(I)/Ni(III) manifold. They further suggest an enantio-determining radical capture event and shed light on the origin of the Dynamic Kinetic Resolution process.
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