C-N Axially Chiral Heterobiaryl Isoquinolinone Skeletons Construction via Cobalt-Catalyzed Atroposelective C-H Activation/Annulation

被引:22
作者
Wang, Xinhai [1 ]
Si, Xiao-Ju [1 ]
Sun, Yingjie [1 ]
Wei, Zhisen [1 ]
Xu, Miao [1 ]
Yang, Dandan [1 ]
Shi, Linlin [1 ]
Song, Mao-Ping [1 ]
Niu, Jun-Long [1 ]
机构
[1] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
ASYMMETRIC-SYNTHESIS; ACTIVATION; ANNULATION; ATROPISOMERS; ALLYLATION; ARYLATION; ANILIDES; ALLENES;
D O I
10.1021/acs.orglett.3c01685
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, the atroposelective construction of isoquinolinonesbearinga C-N chiral axis has been successfully developed via a Co-catalyzedC-H bond activation and annulation process. This conversioncan be effectively carried out in an environmentally friendly oxygenatmosphere to generate the target C-N axially chiral frameworkswith excellent reactivities and enantioselectivities (up to >99%ee)in the absence of any additives. Additionally, the current protocolhas proved to be an alternative approach for the C-N axialarchitectures fabrication under electrochemical conditions for cobalt/Saloxcatalysis, and this strategy allowed the efficient and atom-economicalsynthesis of various axially chiral isoquinolinones under mild reactionconditions.
引用
收藏
页码:6240 / 6245
页数:6
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