Selectively Oxidative C(sp2)-H/C(sp3)-H Cross-Coupling of Benzamides with Amides by Nickel Catalysis

被引:11
作者
Lv, Ningning [1 ]
Yu, Shuling [2 ]
Hong, Chao [2 ]
Han, De-Man [3 ]
Zhang, Yuhong [2 ]
机构
[1] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Peoples R China
[2] Zhejiang Univ, Dept Chem, Hangzhou 310027, Peoples R China
[3] Taizhou Univ, Dept Chem, Jiaojiang 318000, Peoples R China
关键词
C-H BOND; C(SP(3))-H BONDS; ARENES; C(SP(2))-H; ALKENES; FUNCTIONALIZATION; METHYLATION; ACTIVATION; AMINATION; INDOLES;
D O I
10.1021/acs.orglett.0c03535
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The oxidative cross-coupling between the alpha-C(sp(3))-H bond of amide in DMAc and the inert ortho-C(sp(2))-H bond of benzamides is achieved for the first time by nickel catalysis, with the assistance of 8-aminoquinolyi group in the presence of a silver oxidant. Notably, the selectivity of conversion can be perfectly controlled by modulating the oxidant additives, and the products from the coupling of the C(sp(3))-H bond adjacent to nitrogen of amides with benzamides are approached through the use of peroxide.
引用
收藏
页码:9308 / 9312
页数:5
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