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作 者:Ze-Feng Xu Min Jiang Jin-Tao Liu
机构地区:[1]Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China [2]Department of Chemistry, Zhejiang Sci-Tech University, Xiasha West Higher Education District, Hangzhou, Zhejiang 310018, China
出 处:《Chinese Journal of Chemistry》2017年第4期442-446,共5页中国化学(英文版)
基 金:We thank the National Natural Science Foundation of China (No. 21572257 and 21502213) and Shanghai Sailing Program (No. 15YF1414800) for financial support.
摘 要:Several perfluoroalkanesulfenyl chlorides were prepared from the corresponding perfluoroalkanesulfenic acids in high yields, and their reactions with thiol, amine, arene and alkene were studied. A series of perfluoroal- kyl-containing disulfides, sulfonamides, aryl sulfides and a-chlorosulfides were synthesized under mild conditions.Several perfluoroalkanesulfenyl chlorides were prepared from the corresponding perfluoroalkanesulfenic acids in high yields, and their reactions with thiol, amine, arene and alkene were studied. A series of perfluoroal- kyl-containing disulfides, sulfonamides, aryl sulfides and a-chlorosulfides were synthesized under mild conditions.
关 键 词:perfluoroalkanesulfenyl chloride perfluoroalkanesulfenyl acid SUBSTITUTION DISULFIDE ADDITION
分 类 号:TQ153.15[化学工程—电化学工业] TQ028.8
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