Cobalt(II)-Catalyzed Activation of C(sp3)-H Bonds: Organic Oxidant Enabled Selective Functionalization

被引:18
作者
Zhang, He [1 ,2 ]
Sun, Meng-Chan [1 ,2 ]
Yang, Dandan [1 ,2 ]
Li, Tong [1 ,2 ]
Song, Mao-Ping [1 ,2 ]
Niu, Jun-Long [1 ,2 ]
机构
[1] Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R China
关键词
cobalt(II); C(sp(3))-H activation; organic oxidant; selectivity; organometallic Co(III) species; C-H BONDS; CATALYZED ARYLATION; TERMINAL ALKYNES; AMINO-ACIDS; COBALT; AMIDATION; C(SP(2))-H; CYCLIZATION; CARBONYLATION; PICOLINAMIDE;
D O I
10.1021/acscatal.1c05250
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Herein we develop a new "cobalt(II)/organic oxidant" catalytic system for the selective activation of 1 degrees, 2 degrees, and 3 degrees C(sp(3))-H bonds to construct C-N and C-O bonds, respectively. The method highlights the use of an organic compound (TsNHOPiv or its analogues) as an emerging oxidant and thus provides a flexible strategy for the preparation of indoline and benzoxazine derivatives. Attractive advantages of this cobalt catalysis include simple operation, low cost, mild conditions, and broad substrate scope. Furthermore, a catalytically competent hydroxylamine-chelated organometallic Co(III)species was synthesized, thus providing deep insights into the catalytic mechanism.
引用
收藏
页码:1650 / 1656
页数:7
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