胺化
阿托品
对映选择合成
组合化学
化学
催化作用
芳基
有机催化
基质(水族馆)
有机化学
海洋学
地质学
烷基
作者
Xia Wang,Qian‐Jin An,Shao‐Hua Xiang,Shaoyu Li,Yong‐Bin Wang,Bin Tan
标识
DOI:10.1002/anie.202000585
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.
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