Synthesis of Axially Chiral Biaryls through Cobalt(II)-Catalyzed Atroposelective C-H Arylation

被引:19
|
作者
Wu, Yong-Jie [1 ]
Wang, Zhen-Kai [1 ]
Jia, Zhen-Sheng [1 ]
Chen, Jia-Hao [1 ]
Huang, Fan-Rui [1 ]
Zhan, Bei-Bei [1 ]
Yao, Qi-Jun [1 ]
Shi, Bing-Feng [1 ,2 ]
机构
[1] Zhejiang Univ, Ctr Chem Frontier Technol, Dept Chem, Hangzhou 310027, Peoples R China
[2] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Henan, 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
Arylation; Atroposelectivity; C-H Activation; Cobalt; Dynamic Kinetic Asymmetric Transformations; ASYMMETRIC-SYNTHESIS; ARYLBORONIC ACIDS; ATROPISOMERS; CONSTRUCTION; OLEFINATION; ACTIVATION; INDOLE; FUNCTIONALIZATION; ALKYLATION; CATALYST;
D O I
10.1002/anie.202310004
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Highly efficient synthesis of axially chiral biaryl amines through cobalt-catalyzed atroposelective C-H arylation using easily accessible cobalt(II) salt and salicyloxazoline ligand has been reported. This methodology provides a straightforward and sustainable access to a broad range of enantioenriched biaryl-2-amines in good yields (up to 99%) with excellent enantioselectivities (up to 99% ee). The synthetic utility of the unprecedented method is highlighted by its scalability and diverse transformations.
引用
收藏
页数:6
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