PALLADIUM-CATALYZED SELECTIVE α-ARYLATION OF ORTHO-BROMOACETOPHENONES

被引:3
作者
Krishna, Jonnada [1 ]
Reddy, Alavala Gopi Krishna [1 ]
Satyanarayana, Gedu [1 ]
机构
[1] Indian Inst Technol IIT Hyderabad, Dept Chem, Yeddumailaram 502205, Andhra Pradesh, India
关键词
alpha-Arylation; 1-(2-bromophenyl)ethanones; C-H activation; iodo-arenes; Pd-catalysis; CROSS-COUPLING REACTIONS; H BOND FUNCTIONALIZATION; ROOM-TEMPERATURE; ARYL BROMIDES; C-O; REDUCTIVE ELIMINATION; ASYMMETRIC ARYLATION; CARBON-HETEROATOM; HECK REACTION; EFFICIENT;
D O I
10.1080/00397911.2014.880789
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Synthesis of 1-(2-bromophenyl)-2-phenylethanones via an intermolecular Pd-catalyzed alpha-arylation of 1-(2-bromophenyl) ethanones is presented. The method relies on selective C-H activation (alpha-arylation) of relatively more reactive external iodo-arenes as coupling partners without affecting the bromo-substituent. Moreover, the scope and generality of the method has been well studied by employing the reaction with iodo-arenes as coupling partners bearing electron-withdrawing, simple, and electron-donating groups on the aromatic ring.
引用
收藏
页码:2103 / 2111
页数:9
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