亚胺
对映选择合成
化学
吲哚试验
亲核细胞
催化作用
亲核加成
组合化学
有机催化
基质(水族馆)
立体化学
有机化学
海洋学
地质学
作者
Yuxuan Li,Jing Huang,Zhengyu Han,Hai Huang,Biqiong Hong,Jianwei Sun
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-01-02
卷期号:26 (1): 396-400
被引量:2
标识
DOI:10.1021/acs.orglett.3c04070
摘要
Despite the enormous developments in the asymmetric transformations of indole imine methides (IIMs), the remote asymmetric induction involving IIMs remains challenging due to the spatial interaction requirement between the substrate and catalyst. Herein we report the first catalytic asymmetric nucleophilic addition to indole imine 5-methide (5-IIM), the only topological isomer of IIMs whose asymmetric addition remains unknown. Despite the challenging remote stereocontrol, high efficiency and respectable enantioselectivity were achieved to provide access to a range of enantioenriched indole-containing triaryl alkanes.
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