Rhodium(III)-Catalyzed Three-Component Reaction of Imines, Alkynes, and Aldehydes through C-H Activation

被引:57
作者
Huang, Ji-Rong [1 ]
Song, Qiang [1 ]
Zhu, Yu-Qin [1 ]
Qin, Liu [1 ]
Qian, Zhi-Yong [2 ]
Dong, Lin [1 ,2 ]
机构
[1] Sichuan Univ, West China Sch Pharm, Minist Educ, Key Lab Drug Targeting & Drug Delivery Syst, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Collaborat Innovat Ctr Biotherapy, Chengdu 610041, Peoples R China
关键词
C-H activation; cyclization; multicomponent reactions; rhodium; CATALYZED 3+2 ANNULATION; N-SULFONYL KETIMINES; MULTICOMPONENT REACTIONS; BOND FUNCTIONALIZATION; INTERNAL ALKYNES; INTERMOLECULAR HYDROACYLATION; SECONDARY BENZAMIDES; EFFICIENT SYNTHESIS; AROMATIC KETIMINES; FACILE SYNTHESIS;
D O I
10.1002/chem.201404576
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An efficient rhodium(III)-catalyzed tandem three-component reaction of imines, alkynes and aldehydes through C-H activation has been developed. High stereo-and regioselectivity, as well as good yields were obtained in most cases. The simple and atom-economical approach offers a broad scope of substrates, providing polycyclic skeletons with potential biological properties.
引用
收藏
页码:16882 / 16886
页数:5
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