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Visible-Light Photoredox Decarboxylation of Perfluoroarene Iodine(III) Trifluoroacetates for C-H Trifluoromethylation of (Hetero)arenes
被引:112
|作者:
Yang, Bin
[1
]
Yu, Donghai
[2
]
Xu, Xiu-Hua
[1
]
Qing, Feng-Ling
[1
,3
]
机构:
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Ctr Excellence Mol Synth, Key Lab Organofluorine Chem, 345 Lingling Lu, Shanghai 200032, Peoples R China
[2] Donghua Univ, Coll Chem Chem Engn & Biotechnol, 2999 North Renmin Lu, Shanghai 201620, Peoples R China
[3] Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med Res, Minist Educ China, Coll Chem & Chem Engn, Changsha 410081, Hunan, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
trifluoromethylation;
photocatalysis;
decarboxylation;
trifluoroacetic acid;
iodine(III) reagent;
ALPHA-OXOCARBOXYLIC ACIDS;
AROMATIC-COMPOUNDS;
CARBOXYLIC-ACIDS;
KETO ACIDS;
PERFLUOROALKYLATION;
ALKENES;
CATALYSIS;
REAGENTS;
FUNCTIONALIZATION;
DRIVEN;
D O I:
10.1021/acscatal.7b03990
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
A scalable and operationally simple decarboxylative trifluoromethylation of (hetero)arenes with easily accessible C6F5I(OCOCF3)(2) under photoredox catalysis has been developed. This method is tolerant of various (hetero)-arenes and functional groups. Notably, C6F5I is recycled from the decarboxylation reaction and further used for the preparation of C6F5I(OCOCF3)(2). The combination of photoredox catalysis and hypervalent iodine reagent provides a practical approach for the application of trifluoroacetic acid in trifluoromethylation reactions.
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页码:2839 / 2843
页数:9
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