Journal
RSC ADVANCES
Volume 4, Issue 37, Pages 19472-19475Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra02935f
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Funding
- 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]
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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.
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