期刊
RSC ADVANCES
卷 4, 期 37, 页码 19472-19475出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra02935f
关键词
-
资金
- NSFC of China [21202064]
- Jiangxi Provincial Department of Education [GJJ12211]
- Sponsored Program for Cultivating Youths of Outstanding Ability in Jiangxi Normal University
- Zhejiang Provincial Program for the Cultivation of High-level Innovative Health talents
- program of Graduate Student Innovative Research from Jiangxi Province [YC2013-S104]
Selective bis-sulfenylation reactions of aryl dihalides have been achieved by copper-catalyzed C-S coupling reactions under mild conditions of refluxing EtOH (80 degrees C). Employment of disulfides as thiolating reagents enables the production of various bis(phenylthio) benzenes with excellent selectivity, and no products from mono C-S coupling are isolated.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据