Transition-metal-free, visible-light-mediated cyclization of o-azidoarylalkynes with aryl diazonium salts

被引：21
|
作者：
Jin, Cheng [1 ]
Su, Lianzheng [2 ]
Ma, Daxi [3 ]
Cheng, Mingrong [4 ]
机构：
[1] New United Grp Co Ltd, Changzhou 213166, Jiangsu, Peoples R China
[2] Jiangsu Vcare Pharmatech Co Ltd, Nanjing 211800, Jiangsu, Peoples R China
[3] Shanghai Univ Med & Hlth Sci, Affiliated Zhoupu Hosp, Dept Gen Surg, Shanghai 201318, Peoples R China
[4] Tongji Univ, Tianyou Hosp, Dept Gen Surg, Shanghai 200000, Peoples R China
来源：
NEW JOURNAL OF CHEMISTRY | 2017年 / 41卷 / 23期
关键词：
C-H ARYLATION; INDOLE SYNTHESIS; ARYLSULFONYL CHLORIDES; REGIOSPECIFIC ROUTE; N-H; ALKYNES; ANNULATION; CHEMISTRY; EFFICIENT;
D O I：
10.1039/c7nj03144k
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Visible light along with 3 mol% eosin Y catalyzes the cyclization reaction of o-azidoarylalkynes with aryl diazonium salts by a photo-redox process. We have investigated the scope of the reaction for several aryl diazonium salts and o-azidoarylalkynes. The general and easy procedure provides a transition-metal-free alternative for the formation of unsymmetrical 2,3-diaryl-substitued indoles.
引用
收藏
页码：14053 / 14056
页数：4
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