Chiral Phosphoric Acid Catalyzed Atroposelective C-H Amination of Arenes

被引:155
|
作者
Xia, Wang [1 ,2 ]
An, Qian-Jin [1 ,2 ]
Xiang, Shao-Hua [1 ,2 ,3 ]
Li, Shaoyu [1 ,2 ,3 ]
Wang, Yong-Bin [1 ,2 ]
Tan, Bin [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen 518055, Peoples R China
[2] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China
[3] Southern Univ Sci & Technol, Acad Adv Interdisciplinary Studies, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
amination; atropisomerism; chiral phosphoric acid; heterocycles; organocatalysis; FRIEDEL-CRAFTS ALKYLATION; CROSS-COUPLING REACTIONS; MANNICH-TYPE REACTION; N BOND FORMATION; ENANTIOSELECTIVE SYNTHESIS; BIARYL ATROPISOMERS; NATURAL-PRODUCTS; BRONSTED ACID; COPPER; CONSTRUCTION;
D O I
10.1002/anie.202000585
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
N-arylcarbazole structures are important because of their prevalence in natural products and functional OLED materials. C-H amination of arenes has been widely recognized as the most efficient approach to access these structures. Conventional strategies involving transition-metal catalysts suffer from confined substrate generality and the requirement of exogenous oxidants. Organocatalytic enantioselective C-N chiral axis construction remains elusive. Presented here is the first organocatalytic strategy for the synthesis of novel axially chiral N-arylcarbazole frameworks by the assembly of azonaphthalenes and carbazoles. This reaction accommodates broad substrate scope and gives atropisomeric N-arylcarbazoles in good yields with excellent enantiocontrol. This approach not only offers an alternative to metal-catalyzed C-N cross-coupling, but also brings about opportunities for the exploitation of structurally diverse N-aryl atropisomers and OLED materials.
引用
收藏
页码:6775 / 6779
页数:5
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