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手性磷酸催化芳烃的阻转选择性C-H胺化反应

Chiral Phosphoric Acid Catalyzed Atroposelective C-H Amination of Arenes.

作者信息

Xia Wang, An Qian-Jin, Xiang Shao-Hua, Li Shaoyu, Wang Yong-Bin, Tan Bin

机构信息

Shenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, China.

Academy for Advanced Interdisciplinary Studies, Southern University of Science and Technology, Shenzhen, 518055, China.

出版信息

Angew Chem Int Ed Engl. 2020 Apr 20;59(17):6775-6779. doi: 10.1002/anie.202000585. Epub 2020 Mar 3.

Abstract

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.

摘要

N-芳基咔唑结构因其在天然产物和功能性有机发光二极管材料中的广泛存在而具有重要意义。芳烃的C-H胺化反应已被广泛认为是获得这些结构的最有效方法。涉及过渡金属催化剂的传统策略存在底物通用性受限和需要外源氧化剂的问题。有机催化对映选择性C-N手性轴构建仍然难以实现。本文介绍了第一种通过氮杂萘和咔唑的组装合成新型轴向手性N-芳基咔唑骨架的有机催化策略。该反应具有广泛的底物范围,能以良好的收率和优异的对映体控制得到阻转异构的N-芳基咔唑。这种方法不仅为金属催化的C-N交叉偶联提供了一种替代方案,还为开发结构多样的N-芳基阻转异构体和有机发光二极管材料带来了机遇。

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