CpxM(iii)-catalyzed enantioselective C-H functionalization through migratory insertion of metal-carbenes/nitrenes

被引:28
|
作者
Pan, Chongqing [1 ]
Yin, Si-Yong [1 ]
Gu, Qing [1 ]
You, Shu-Li [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, 345 Lingling Lu, Shanghai 200032, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
PLANAR CHIRAL FERROCENES; BOND FUNCTIONALIZATION; ASYMMETRIC CATALYSIS; LIGANDS; RH(III); ACTIVATION; RH; AMIDATIONS; COMPLEXES;
D O I
10.1039/d1ob01248g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
(CpM)-M-x(iii)-catalyzed enantioselective C-H functionalization reactions have progressed rapidly using either chiral cyclopentadienyl ligands or appropriate chiral carboxylic acids. In this context, highly reactive carbene and nitrene precursors can serve as effective C-H coupling partners, providing a straightforward and efficient approach to access chiral molecules. In this review, we highlight the developments in (CpM)-M-x(iii)-catalyzed enantioselective C-H functionalization reactions through migratory insertion of metal-carbenes/nitrenes by employing chiral (CpM)-M-x(iii) complexes or achiral (CpM)-M-x(iii) complexes combined with chiral carboxylic acids.
引用
收藏
页码:7264 / 7275
页数:12
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