Electrochemical synthesis of 3-azido-indolines from amino-azidation of alkenes

被引:34
作者
Guo, Shengping [1 ,2 ,3 ]
Liu, Liyan [1 ,2 ,3 ]
Hu, Kangfei [1 ,2 ,3 ]
Sun, Qi [1 ,2 ,3 ]
Zha, Zhenggen [1 ,2 ,3 ]
Yang, Yu [4 ]
Wang, Zhiyong [1 ,2 ,3 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Soft Matter Chem, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
[2] Univ Sci & Technol China, Ctr Excellence Mol Synth, Chinese Acad Sci, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Hefei 230026, Peoples R China
[3] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei 230026, Peoples R China
[4] Hefei Normol Univ, Sch Chem & Chem Engn, Hefei 230601, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Electrochemical; Amino-azidation; 2-Aminostyrene; Metal-free; Oxidant-free; 3-Azido indolines; C-H FUNCTIONALIZATION; OXIDATIVE ANNULATION; ORGANIC AZIDES; BOND FORMATION; CHEMISTRY; CYCLIZATION; STRATEGIES; AZIRIDINES; CATALYSIS;
D O I
10.1016/j.cclet.2020.09.041
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An electrochemical amino-azidation of 2-aminostyrene with sodium azide (NaN3) was developed, which can be carried out smoothly in water under metal-free condition, affording a series of 3-azido indolines with high yields. (C) 2020 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1033 / 1036
页数:4
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