期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 77, 期 22, 页码 10369-10374出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo302088t
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资金
- National Science Council, Taiwan [NSC 101-2113-M-005-008-MY3]
- National Chung Hsing University
A convenient one-pot approach for the synthesis of aryl sulfides through the coupling of thiols with Grignard reagents in the presence of N-chlorosuccinimide is described. The sulfenylchlorides were formed when thiols were treated with N-chlorosuccinimide, and the resulting sulfenylchlorides were then directly reacted with Grignarcl reagents to provide aryl sulfides in good to excellent yields under mild reaction conditions. Functional groups including ester, fluoro, and chloro are tolerated by the reaction conditions employed. It is important to note that this method has a short reaction time (30 min in total) and represents an alternative approach for the synthesis of aryl sulfides over the existing protocols.
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