Electrochemical synthesis of 6-arylsulfonyl caffeic acid derivatives in aqueous medium

被引：32
|
作者：
Zeng, Cheng-Chu [1 ]
Liu, Cheng-Fu [1 ]
Zeng, Jia [1 ]
Zhong, Ru-Gang [1 ]
机构：
[1] Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100022, Peoples R China
来源：
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 2007年 / 608卷 / 02期
基金：
中国国家自然科学基金;
关键词：
caffeic acid; benzenesulfinate; organic electrochemical synthesis; cyclic voltammetry;
D O I：
10.1016/j.jelechem.2007.02.005
中图分类号：
O65 [分析化学];
学科分类号：
070302 ; 081704 ;
摘要：
The anodic oxidation of caffeic acid in the presence of sodium benzenesulfinate in aqueous solution was studied by cyclic voltammetry and controlled potential coulometry. The results showed that similar to other simple catechol derivatives where the substituents attached directly to the benzene ring, caffeic acid was oxidized to the corresponding o-benzoquinone which underwent further Michael-addition with sodium benzenesulfinate or sodium p-methyl benzenesulfinate to produce 6-arylsulfonyl caffeic acid derivative 7a or 7b. (c) 2007 Published by Elsevier B.V.
引用
收藏
页码：85 / 90
页数：6
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