Iridium(III)-catalyzed regioselective direct arylation of sp2 C-H bonds with diaryliodonium salts

被引:23
|
作者
Gao, Pan [1 ,2 ]
Liu, Li [3 ]
Shi, Zhuangzhi [2 ]
Yuan, Yu [1 ]
机构
[1] Yangzhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Life Sci, State Key Lab Coordinat Chem, Nanjing 210093, Jiangsu, Peoples R China
[3] Changzhou Univ, Sch Petrochem Engn, Changzhou 213164, Peoples R China
关键词
ENANTIOSELECTIVE ALPHA-ARYLATION; CROSS-COUPLING REACTIONS; AMINO-GROUPS; IRIDIUM; AMIDATION; MILD; FUNCTIONALIZATION; ARENES; ACTIVATION; ALKENES;
D O I
10.1039/c6ob01145d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A regioselective direct arylation of arenes and olefins at the ortho position is reported. The key to the high selectivity is the appropriate choice of diaryliodonium salts as the arylating reagent in the presence of a cationic iridium(III) catalyst. The coordination of the metal with an oxygen atom or a nitrogen atom and subsequent C-H activation allows for direct arylation with coupling partners. This reaction proceeds under mild reaction conditions and with a high tolerance of various functional groups including many halide functional groups.
引用
收藏
页码:7109 / 7113
页数:5
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