阿托品
对映选择合成
化学
铱
烷基化
组合化学
催化作用
吡咯
吲哚试验
立体化学
有机化学
作者
Si‐Yong Yin,Qiansujia Zhou,Chen‐Xu Liu,Qing Gu,Shu-Li You
标识
DOI:10.1002/anie.202305067
摘要
Enantioselective synthesis of N-N biaryl atropisomers is an emerging area but remains underexplored. The development of efficient synthesis of N-N biaryl atropisomers is in great demand. Herein, the construction of N-N biaryl atropisomers through iridium-catalyzed asymmetric C-H alkylation is reported for the first time. In the presence of readily available Ir precursor and Xyl-BINAP, a variety of axially chiral molecules based on indole-pyrrole skeleton were obtained in good yields (up to 98 %) with excellent enantioselectivity (up to 99 % ee). In addition, N-N bispyrrole atropisomers could also be synthesized in excellent yields and enantioselectivity. This method features perfect atom economy, wide substrate scope, and multifunctionalized products allowing diverse transformations.
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