Electrochemical synthesis of selenocyanated imidazo[1,5-a]quinolines under metal catalyst-and chemical oxidant-free conditions

被引:6
|
作者
Jinjin Zhang [1 ]
Huiqiao Wang [1 ]
Yaru Chen [1 ]
Haiquan Xie [1 ]
Chenghua Ding [1 ]
Jiajing Tan [2 ]
Kun Xu [1 ,3 ]
机构
[1] College of Chemistry and Pharmaceutical Engineering, Nanyang Normal University
[2] Department of Organic Chemistry, Faculty of Chemistry, Beijing University of Chemical Technology
[3] College of Life Science & Bioengineering, Beijing University of Technology
基金
中央高校基本科研业务费专项资金资助; 北京市自然科学基金; 中国国家自然科学基金; 河南省教育厅基金;
关键词
Electrosynthesis; Organic electrochemistry; Anodic oxidation; Imidazo[1,5-a]quinoline; Selenocyanation;
D O I
暂无
中图分类号
O626 [杂环化合物];
学科分类号
070303 ; 081704 ;
摘要
Reported herein is the first example of electrochemical selenocyanation of imidazo[1,5-a]quinolines with KSeCN under metal catalyst-and chemical oxidant-free conditions.This sustainable strategy shows a broad scope and great compatibility with functional groups,and affords synthetically and biologically important selenocyanated imidazo[1,5-a]quinolines in good to excellent yields with cheap graphite and Ni plates as the electrodes.The gram-scale synthesis was also successfully conducted,which might demonstrate the potential value of this electrochemical protocol.
引用
收藏
页码:1576 / 1579
页数:4
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