Computational and experimental studies on copper-mediated selective cascade C-H/N-H annulation of electron-deficient acrylamide with arynes

被引:33
作者
Chen, Chao [1 ,2 ]
Hao, Yu [1 ,2 ]
Zhang, Ting-Yu [1 ,2 ]
Pan, Jin-Long [1 ,2 ]
Ding, Jun [1 ,2 ]
Xiang, Heng-Ye [1 ,2 ]
Wang, Man [1 ,2 ]
Ding, Tong-Mei [1 ,2 ]
Duan, Abing [3 ]
Zhang, Shu-Yu [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Key Lab Mol Engn Chiral Drugs, Peoples Hosp South Campus 6, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[3] Hunan Univ, Coll Environm Sci & Technol, Changsha 410082, Hunan, Peoples R China
关键词
N-METHOXYBENZAMIDES; DIRECTING-GROUP; OXIDATIVE CYCLOADDITION; SULFOXONIUM YLIDES; BOND ACTIVATION; BENZAMIDES; ARYLATION; FUNCTIONALIZATION; ACIDS; PHENANTHRIDINONES;
D O I
10.1039/c8cc08708c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An efficient and convenient copper-mediated method has been developed to achieve direct cascade C-H/N-H annulation to synthesize 2-quinolinones from electron-deficient acrylamides and arynes. This method highlights an emerging but simple strategy to transform inert C-H bonds into versatile functional groups in organic synthesis to provide a new method of synthesizing 2-quinolinones efficiently. Mechanistic investigations by experimental and density functional theory (DFT) studies suggest that an organometallic C-H activation via a Cu(III) intermediate is likely to be involved in the reaction.
引用
收藏
页码:755 / 758
页数:4
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