Isolation, Structure, and Reactivity of an Arylnickel(II) Pivalate Complex in Catalytic C-H/C-O Biaryl Coupling

被引:140
作者
Muto, Kei [1 ,2 ]
Yamaguchi, Junichiro [1 ,2 ]
Lei, Aiwen [4 ]
Itami, Kenichiro [1 ,2 ,3 ]
机构
[1] Nagoya Univ, Inst Transformat Biomol WPI ITbM, Nagoya, Aichi 4648602, Japan
[2] Nagoya Univ, Grad Sch Sci, Nagoya, Aichi 4648602, Japan
[3] Nagoya Univ, JST, ERATO, Itami Mol Nanocarbon Project, Nagoya, Aichi 4648602, Japan
[4] Wuhan Univ, Coll Chem, Wuhan 430072, Peoples R China
关键词
H BOND FUNCTIONALIZATION; N-AROMATIC HETEROCYCLES; DIRECT ARYLATION; ACTIVATION; AZOLES; MECHANISM; HETEROARENES; CLEAVAGE; ALKENYLATION; ALKYLATION;
D O I
10.1021/ja409803x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe mechanistic studies of a C-H/C-O biaryl coupling of 1,3-azoles and aryl pivalates catalyzed by Ni(cod)(2)/dcype. This study not only supports a catalytic cycle consisting of C-O oxidative addition, C-H nickelation, and reductive elimination but also provides insight into the dramatic ligand effect in C-H/C-O coupling. We have achieved the first synthesis, isolation and structure elucidation of an arylnickel(II) pivalate, which is an intermediate in the catalytic cycle after oxidative addition of a C-O bond. Furthermore, kinetic studies and kinetic isotope effect investigations reveal that the C-H nickelation is the turnover-limiting step in the catalytic cycle.
引用
收藏
页码:16384 / 16387
页数:4
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