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Radical Carbofluorination of Unactivated Alkenes with Fluoride Ions

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NIAID Data Ecosystem2026-03-10 收录
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https://figshare.com/articles/dataset/Radical_Carbofluorination_of_Unactivated_Alkenes_with_Fluoride_Ions/6227426
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The copper-assisted radical carbofluorination of unactivated alkenes with fluoride ions is described. With [Cu­(L3)­F2]­H2O (L3 = 4,4′-di­(methoxycarbonyl)-2,2′-bipyridine) as the fluorine source and [Ag­(DMPhen)­(MeCN)]­BF4 (DMPhen = 2,9-dimethyl-1,10-phenanthroline) as the chloride scavenger, the reaction of unactivated alkenes with CCl4 in acetonitrile provided the corresponding carbofluorination products in satisfactory yields. The protocol exhibited a wide functional group compatibility and broad substrate scope and could be extended to the use of a variety of activated alkyl chlorides other than CCl4. A copper-catalyzed fluorotrifluoromethylation of unactivated alkenes was then successfully developed with CsF as the fluorine source and Umemoto’s reagent as the trifluoromethylating agent. A mechanism involving the fluorine atom transfer from Cu­(II)–F complexes to alkyl radicals is proposed.
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2018-05-07
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