Synthesis of 2-Arylbenzoselenazoles by Sulfur-Mediated Cyclization of Bis(2-aminophenyl) Diselenide and Benzyl Chlorides

被引：0
|
作者：
Guo, X. H. [1 ]
Wu, H. L. [1 ]
Gan, H. F. [1 ]
机构：
[1] Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Peoples R China
来源：
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY | 2023年 / 59卷 / 04期
基金：
中国国家自然科学基金;
关键词：
benzyl chloride; 1; 3-benzoselenazoles; bis(2-aminophenyl) diselenide; cyclization; sulfur; ONE-POT SYNTHESIS; REDOX CONDENSATION; 1,2-DISUBSTITUTED BENZIMIDAZOLES; S-8-MEDIATED CYCLIZATION; SELENIUM; BENZOXAZOLES; DERIVATIVES; BENZOTHIAZOLES; EBSELEN; AGENTS;
D O I：
10.1134/S1070428023040206
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A metal-free S-8-mediated cyclization of bis(2-aminophenyl) diselenide and benzyl chlorides to synthesize 2-arylbenzoselenazoles has been proposed. The reactions provided moderate to good yields with good functional tolerance.
引用
收藏
页码：704 / 711
页数：8
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