Publication | Closed Access
Visible-Light-Mediated Fluoroalkylation of Isocyanides with Ethyl Bromofluoroacetates: Unified Synthesis of Mono- and Difluoromethylated Phenanthridine Derivatives
239
Citations
50
References
2014
Year
Combinatorial ChemistryEngineeringUnified StrategyOrganic ChemistryChemistryHeterocycle ChemistryChemical DerivativeMedicinal ChemistryBiphenyl IsocyanidesDifluoromethylated Phenanthridine DerivativesDerivative (Chemistry)PhotochemistryVisible-light-mediated FluoroalkylationFluorous SynthesisPharmacologyBiomolecular EngineeringRoom TemperatureHeterocyclicNatural SciencesEthyl BromofluoroacetatesSynthetic Chemistry
A practical and unified strategy has been described for the preparation of mono- and difluoromethylated phenanthridine derivatives using a visible-light-promoted alkylation and decarboxylation sequence from biphenyl isocyanides with ethyl bromofluoroacetate (EBFA) or ethyl bromodifluoroacetate (EBDFA). These reactions could be carried out at room temperature in good to excellent chemical yields. Both stepwise and one-pot procedures have been developed, which makes this strategy more attractive.
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