Journal of the American Chemical Society · 2013 · 217 citations · 20 references
Natural SciencesChemistryAnalytical ChemistryInorganic ChemistryOrganometallic ChemistryCoordination ChemistryMetal-ligand BondingReductive EliminationCopper-catalyzed OxidationCopper-mediated OxidationFluorination ProcessesMild Reaction ConditionsOxidationReductive Elimination From Copper ComplexesReductive Elimination MechanismTandem Reactions
A method for the direct conversion of arylboronate esters to aryl fluorides under mild conditions with readily available reagents is reported. Tandem reactions have also been developed for the fluorination of arenes and aryl bromides through arylboronate ester intermediates. Mechanistic studies suggest that this fluorination reaction occurs through facile oxidation of Cu(I) to Cu(III), followed by rate-limiting transmetalation of a bound arylboronate to Cu(III). Fast C-F reductive elimination is proposed to occur from an aryl-copper(III)-fluoride complex. Cu(III) intermediates have been generated independently and identified by NMR spectroscopy and ESI-MS.
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George A. Olah, John T. Welch, Yashwant D. Vankar et al. · The Journal of Organic Chemistry · 1979 · 566 citations
Fluorination of Boronic Acids Mediated by Silver(I) Triflate
Takeru Furuya, Tobias Ritter · Organic Letters · 2009 · 302 citations