共 50 条
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.
引用
下载
收藏
页码:809 / 814
页数:6
相关论文