Nickel-catalyzed allylic defluorinative alkylation of trifluoromethyl alkenes with reductive decarboxylation of redox-active esters

被引:177
|
作者
Lu, Xi [1 ]
Wang, Xiao-Xu [1 ]
Gong, Tian-Jun [1 ]
Pi, Jing-Jing [1 ]
He, Shi-Jiang [1 ]
Fu, Yao [1 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Urban Pollutant Convers, Anhui Prov Key Lab Biomass Clean Energy,iChEM, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
N-HYDROXYPHTHALIMIDE ESTERS; F BOND ACTIVATION; GEM-DIFLUOROALKENES; DIAZO-COMPOUNDS; EFFICIENT APPROACH; COUPLING REACTIONS; ARYL BROMIDES; FLUORINE; HALIDES; DIFLUOROOLEFINATION;
D O I
10.1039/c8sc04335c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we report a nickel-catalyzed allylic defluorinative alkylation of trifluoromethyl alkenes through reductive decarboxylation of redox-active esters. The present reaction enables the preparation of functionalized gem-difluoroalkenes with the formation of sterically hindered C(sp(3))-C(sp(3)) bonds under very mild reaction conditions, while tolerating many sensitive functional groups and requiring minimal substrate protection. Therefore, this method provides an efficient and convenient approach for late-stage modification of biologically interesting molecules.
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页码:809 / 814
页数:6
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