Electrochemical synthesis of benzoxazoles mediated by 2,3-dichloro-5,6-dicyano-p-hydroquinone (DDH) as a redox catalyst

被引：16

作者：

Kang, Li-Shuo ^{[1
]}

Xiao, Huan-lan ^{[1
]}

Zeng, Cheng-Chu ^{[1
]}

Hu, Li-Ming ^{[1
]}

Little, R. Daniel ^{[2
]}

机构：

[1] Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100124, Peoples R China

[2] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA

来源：

JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 2016年 / 767卷

基金：

美国国家科学基金会; 中国国家自然科学基金;

关键词：

Indirect electrolysis; 2,3-Dichloro-5,6-dicyano-p-hydroquinone (DDH); 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ); Benzoxazole; Schiff base; C-H BONDS; 2-SUBSTITUTED BENZOXAZOLES; FACILE PREPARATION; POWERFUL CATALYST; OXIDATION; TRIARYLIMIDAZOLE; BENZOTHIAZOLES; ARYLATION; POTENT; BENZIMIDAZOLES;

D O I：

10.1016/j.jelechem.2015.12.051

中图分类号：

O65 [分析化学];

学科分类号：

070302 ; 081704 ;

摘要：

A novel electrochemical strategy for the efficient synthesis of benzoxazoles has been developed. The chemistry is performed in a beaker-type undivided cell under constant current electrolysis conditions, utilizing 2,3-dichloro-5,6-dicyano-p-hydroquinone (DDH) as a redox catalyst. (C) 2016 Elsevier B.V. All rights reserved.

引用

页码：13 / 17

页数：5

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