Perfluoroalkylation of Thiosulfonates: Synthesis of Perfluoroalkyl Sulfides

被引:26
|
作者
Luo, Ziwei [1 ]
Yang, Xinkan [1 ]
Tsui, Gavin Chit [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China
关键词
METAL-FREE TRIFLUOROMETHYLTHIOLATION; ARYL BORONIC ACIDS; DECARBOXYLATIVE TRIFLUOROMETHYLTHIOLATION; CATALYZED TRIFLUOROMETHYLTHIOLATION; SILVER(I) TRIFLUOROMETHANETHIOLATE; NUCLEOPHILIC TRIFLUOROMETHYLATION; SUBSTITUENT CONSTANTS; TERMINAL ALKYNES; FLUORINE; TRIMETHYLSILANE;
D O I
10.1021/acs.orglett.0c02235
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A practical synthesis of perfluoroalkyl sulfides is described. The method employs stable and readily accessible thiosulfonates as new electrophiles with commercial nucleophilic perfluoroalkylating reagents. The mild reaction conditions allow access to a wide variety of both aryl- and alkyl-substituted perfluoroalkyl sulfides amenable to pharmaceutical development. Furthermore, the reaction operation is straightforward, odorless, does not produce toxic wastes, and, therefore should appeal to practitioners in industrial-scale productions.
引用
收藏
页码:6155 / 6159
页数:5
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