Nickel-Catalyzed Difluoroalkylation of (Hetero)aryl Bromides with Unactivated 1-Bromo-1,1-difluoroalkanes

被引:16
|
作者
He, Xu [1 ]
Gao, Xing [1 ]
Zhang, Xingang [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Ctr Excellence Mol Synth, Key Lab Organofluorine Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
arylbromides; 1-bromo-1; 1-difluoroalkanes; cross-coupling; difluoroalkylations; fluorine; nickel; AROMATIC-COMPOUNDS; HALIDES; ELECTROPHILES; INHIBITORS; TRIFLUOROMETHYLATION; FLUOROALKYLATION; ACTIVATION; CHEMISTRY; FLUORINE; ARENES;
D O I
10.1002/cjoc.201800276
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although extensive efforts on fluoroalkylations have been made over the past decade, new and efficient methods to incorporate fluorinated groups into organic molecules remain highly desirable. Herein, we report an efficient method for catalytic synthesis of difluoroalkylated (hetero)arenes through nickel-catalyzed reaction between readily accessible (hetero)aryl bromides and unactivated 1-bromo-1,1-difluoroalkanes. The reaction exhibits high functional group tolerance and broad substrate scope, providing a cost-efficient and straightforward route for applications in medicinal chemistry.
引用
收藏
页码:1059 / 1062
页数:4
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