共 51 条
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.
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页码:16384 / 16387
页数:4
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