Publication | Closed Access
Xenon Difluoride Mediated Fluorodecarboxylations for the Syntheses of Di- and Trifluoromethoxyarenes
63
Citations
46
References
2016
Year
Positron Emission TomographyElectron-poor SubstratesEngineeringBiochemistryNatural SciencesFluorous SynthesisOrganic ChemistryFuture Pet-imaging ApplicationsChemistryProficient Fluorine-transfer ReagentHalogenationDerivative (Chemistry)Molecular ImagingBiomolecular Engineering
XeF2 is demonstrated to be a more proficient fluorine-transfer reagent than either NFSI or Selectfluor in fluorodecarboxylations of both mono- and difluoroaryloxy acetic acid derivatives. This method efficiently converts a wide range of neutral and electron-poor substrates to afford the desired di- and trifluoromethyl aryl ethers in good to excellent yields. The purifications are facile, and the reaction times are less than 5 min, which makes these fluorodecarboxylations promising for future PET-imaging applications.
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