Copper-catalyzed radical trifluoromethylalkynylation of unactivated alkenes with terminal alkynes

被引:6
|
作者
Ren, Yang-Qing [1 ,2 ,3 ]
Yang, Chang-Jiang [1 ]
Li, Zhong-Liang [4 ,5 ]
Gu, Qiang-Shuai [4 ]
Liu, Lin [1 ]
Liu, Xin-Yuan [2 ,3 ]
机构
[1] Great Bay Univ, Inst Sci Res, Sch Sci, Dongguan 523000, Peoples R China
[2] Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen 518055, Peoples R China
[3] Southern Univ Sci & Technol, Dept Chem, Guangdong Prov Key Lab Catalysis, Shenzhen 518055, Peoples R China
[4] Southern Univ Sci & Technol, Acad Adv Interdisciplinary Studies, Shenzhen 518055, Peoples R China
[5] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
Trifluoromethylalkynylation; Terminal alkyne; Radical reaction; Copper; Unactivated alkenes; C-H BONDS; FLUORINE; ALKYNYLATION; 1,2-DIFUNCTIONALIZATION; 1,2-ADDITION; ELIMINATION; STYRENES; BROMIDES; IODIDES; SILVER;
D O I
10.1016/j.jfluchem.2023.110107
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A copper-catalyzed three-component radical trifluoromethylalkynylation of unactivated alkenes is realized from Togni-II reagent and readily available terminal alkynes under mild conditions to afford an array of beta-tri- fluoromethylated alkynes. The utilization of a multidentate N,N,N-ligand is crucial for the efficient radical generation and the C(sp3)-C(sp) bond formation. Facile transformations of the difunctionalization products highlight its potential utility in the synthesis of various trifluoromethyl-containing building blocks.
引用
收藏
页数:6
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