化学
烯丙基重排
赫克反应
对映选择合成
催化作用
芳基
产量(工程)
三氟甲基
组合化学
电泳剂
镍
药物化学
级联反应
有机化学
钯
烷基
冶金
材料科学
作者
Yuanyuan Hu,Xiao-Qiu Xu,Wei-Chao Deng,Ren‐Xiao Liang,Yi‐Xia Jia
出处
期刊:Organic Letters
[American Chemical Society]
日期:2023-08-14
卷期号:25 (33): 6122-6127
被引量:12
标识
DOI:10.1021/acs.orglett.3c02092
摘要
Herein, we describe a nickel-catalyzed asymmetric dearomative aryl-difluoroallylation reaction of indoles with α-trifluoromethyl alkenes as an electrophilic coupling partner. The reaction proceeds via a cascade sequence involving dearomative Heck cyclization and reductive allylic defluorination. A series of gem-difluoroallyl substituted indolines are obtained in moderate to good yields (36-77% yield) with excellent enantioselectivity (up to 99% ee). The reaction features broad functional group tolerance, scaled-up synthesis, and late-stage diversification.
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