| Literature DB >> 32648444 |
Ziwei Luo1, Xinkan Yang1, Gavin Chit Tsui1.
Abstract
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.Entities:
Year: 2020 PMID: 32648444 DOI: 10.1021/acs.orglett.0c02235
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005