Rh(III)-Catalyzed, Redox-Neutral, C-H Multifluoroalkenylation of Benzamides

被引:0
|
作者
Lin, Wei [1 ]
Qu, Yifei [1 ]
Zhu, Huixuan [1 ]
Xie, Mei [1 ]
Hu, Jinhui [1 ]
Xiong, Zhuang [1 ]
Chen, Wen-Hua [1 ]
Xu, Jun [2 ]
Wu, Jia-Qiang [1 ]
机构
[1] Wuyi Univ, Sch Pharm & Food Engn, Jiangmen 529020, Peoples R China
[2] Sun Yat sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Peoples R China
来源
SYNTHESIS-STUTTGART | 2024年 / 56卷 / 19期
关键词
C-H activation; rhodium; multifluoroalkenylation; benzamide; redox-neutral; ALPHA-FLUOROALKENYLATION; ASYMMETRIC FLUORINATION; PERFLUOROALKYLATION; TRIFLUOROMETHYLATION; FUNCTIONALIZATION; ACCESS;
D O I
10.1055/a-2343-0676
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Fluorinated molecules are widely used in pharmaceutical and agrochemical industries. Multifluoroalkyl-containing compounds have attracted increasing attention for their unique ability to alter the activity of drugs and bioactive molecules. Herein, we report an efficient Rh(III)-catalyzed, redox-neutral, C-H multifluoroalkenylation of benzamides with multifluoroalkenes, which provides a versatile protocol for accessing a wide range of multifluoroalkenylated arenes.
引用
收藏
页码:3045 / 3053
页数:9
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