ACS Omega · 2021 · 18 citations · 48 references
Natural SciencesChemistryMedicinal ChemistryGreen ChemistryReaction EngineeringSynthetic Medicinal ChemistryDiversity-oriented SynthesisHalogen ChemistryHeterocycle SynthesisHeterocyclic ChemistrySafer Chemical SynthesisFunctional Group ToleranceIodine ChemistryQuinoline ChemistryQuinoline SynthesisQuinone ChemistryRegioselectivityRoom-temperature Synthesis
A simple and practical protocol for the C3-H regioselective halogenation of 4-quinolones by the action of potassium halide salt and PIFA/PIDA in good to excellent yields was developed. The current approach provides feasible access to the diversity of C3-halgenated 4-quinolones at room temperature with high regioselectivity and good functional group tolerance, from which bioactive compounds can be easily constructed. Moreover, the current method featured eco-friendly, operational convenience and is suitable for halogenation in a gram scale of 4-quinolones in water without sacrificing yields.
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Chandrakala Pidathala, Richard K. Amewu, Bénédicte Pacorel et al. · Journal of Medicinal Chemistry · 2012 · 110 citations · Full text