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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.
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页数:6
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