Investigations into Transition-Metal-Catalyzed Arene Trifluoromethylation Reactions

被引:163
作者
Ye, Yingda [1 ]
Sanford, Melanie S. [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
关键词
trifluoromethylation; cross-coupling; palladium; silver; photocatalysis; FORMING REDUCTIVE ELIMINATION; COPPER-MEDIATED TRIFLUOROMETHYLATION; OXIDATIVE TRIFLUOROMETHYLATION; BORONIC ACIDS; HETEROAROMATIC-COMPOUNDS; PALLADIUM(IV) COMPLEXES; PHOTOREDOX CATALYSIS; MEDICINAL CHEMISTRY; AROMATIC-COMPOUNDS; ROOM-TEMPERATURE;
D O I
10.1055/s-0032-1316988
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Trifluoromethyl-substituted arenes and heteroarenes are widely prevalent in pharmaceuticals and agrochemicals. As a result, the development of practical methods for the formation of aryl-CF3 bonds has become an active field of research. Over the past five years, transition-metal-catalyzed cross-coupling between aryl-X (X = halide, organometallic, or H) and various 'CF3' reagents has emerged as a particularly attractive approach to generating aryl-CF3 bonds. Despite many recent advances in this area, current methods generally suffer from limitations such as poor generality, harsh reaction conditions, the requirement for stoichiometric quantities of metals, and/or the use of costly CF3 sources. This Account describes our recent efforts to address some of these challenges by: (1) developing aryltrifluoromethylation reactions involving high oxidation state Pd intermediates, (2) exploiting AgCF3 for C-H trifluoromethylation, and (3) achieving Cu-catalyzed trifluoromethylation with photogenerated CF3 center dot.
引用
收藏
页码:2005 / 2013
页数:9
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