Visible-light-induced C-H sulfenylation of quinoxalin-2(1H)-ones with disulfides by sustainable cerium catalysis

被引：16
|
作者：
Zhang, Lixi [1 ,2 ]
Zhang, Pengfei [2 ,3 ]
Zhu, Dancheng [1 ]
Zheng, Kai [1 ]
Shen, Chao [1 ]
机构：
[1] Zhejiang Shuren Univ, Coll Biol & Environm Engn, Key Lab Pollut Exposure & Hlth Intervent Zhejiang, Hangzhou 310015, Peoples R China
[2] Zhejiang Univ Technol, Coll Environm, Hangzhou 310032, Zhejiang, Peoples R China
[3] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Key Lab Organosilicon Chem & Mat Technol, Minist Educ, Hangzhou 311121, Peoples R China
来源：
GREEN SYNTHESIS AND CATALYSIS | 2023年 / 4卷 / 03期
基金：
中国国家自然科学基金;
关键词：
Quinoxalin-2(1 H )-ones; Disulfides; Sulfenylation; Visible light; Cerium catalysis; CARBOXYLIC-ACIDS; BOND FORMATION; PHOTOCATALYST; FUNCTIONALIZATION; ARYLATION; METAL;
D O I：
10.1016/j.gresc.2022.04.004
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Using visible light as energy to form free radicals has important synthetic value. A novel and efficient visible-light -mediated strategy has been developed for the generation of thiobenzene radicals through cerium-catalyzed activation of the disulfides. Through this photochemical reaction, various 3-sulfenylated quinoxalin-2(1H)-ones can be conveniently obtained in good yields with good functional group tolerance. Our transformation provides an alternative that allows rapid access to various C3 sulfenylated quinoxalin-2(1H)-ones in a sustainable and practical manner.
引用
收藏
页码：226 / 230
页数：5
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