化学
烷基化
吲哚试验
区域选择性
铑
吡咯
催化作用
组合化学
有机化学
药物化学
弗里德尔-克拉夫茨反应
作者
Shuang‐Liang Liu,Zhao Ru,Menglong Li,Haoran Yang,Liming Zhou,Shao‐Ming Fang
出处
期刊:Organic Letters
[American Chemical Society]
日期:2023-02-28
卷期号:25 (9): 1375-1379
被引量:9
标识
DOI:10.1021/acs.orglett.3c00057
摘要
The Rh(III)-catalyzed addition of the indole C2–H bond to nitroalkenes under an ambient atmosphere is disclosed, providing direct access to a wide range of 2-(2-nitroalkyl)indoles (33 examples) with excellent chemo- and regioselectivity. In addition, pyrrole derivatives also successfully participated in this Friedel–Crafts alkylation reaction. Representative nitroalkane products could be converted into structurally diverse and valuable indole derivatives. Furthermore, a series of control experiments were conducted, and a plausible mechanism was proposed.
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