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A new synthesis of α-fluoro-α,β-unsaturated ketones and esters based on organoselenium methodology
30
Citations
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References
1992
Year
HalogenationBioorganic ChemistryOrganoselenium MethodologyEngineeringNatural SciencesHydrogen PeroxidePhenylselenenyl BromideFluorous SynthesisOrganic ChemistryNew SynthesisSynthetic ChemistryChemistryPharmacologyβ-Unsaturated KetonesEnantioselective SynthesisBiomolecular EngineeringPhenylselenenyl Fluoride Equivalent
Fluoroselenenylation of α-diazoketones and α-diazoesters using a phenylselenenyl fluoride equivalent, generated in situ from phenylselenenyl bromide and AgF, followed by oxidation with hydrogen peroxide, provided α-fluoro-α,β-unsaturated ketones and ester, respectively, in moderate yields.
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