Journal
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
Volume 13, Issue -, Pages 2626-2630Publisher
BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.13.260
Keywords
alkynes; nucleophilic addition; perfluoroalkylselenolation; Se-trifluoromethyl) 4-methylbenzenesulfonoselenoate; trifluoromethylselenolation
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Funding
- la Region Rhone Alpes
- CNRS
- French Ministry of Research
- French Fluorine Network
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Herein the nucleophilic addition of Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate, a stable and easy-to-handle reagent, to alkynes is described. This reaction provides trifluoromethylselenylated vinyl sulfones with good results and the method was extended also to higher fluorinated homologs. The obtained compounds are valuable building blocks for further syntheses of fluoroalkylselenolated molecules.
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