The Journal of Organic Chemistry · 2021 · 19 citations · 54 references
Natural SciencesChemical EngineeringChemistryGreen ChemistryOrganic ChemistryReaction EngineeringHeterocycle SynthesisOrganic SynthesisSafer Chemical SynthesisSolvent-free SynthesisAldehydesKetonesPyridine ChemistryPyridine SynthesisPyrrole ChemistryPyrrole SynthesisSustainable Reaction EngineeringSustainable Synthesis
A one-pot, four-component annulation of 2,3,4,6-tetraarylpyridines from aromatic aldehydes, methyl ketones, diaryl ethanones, and ammonium acetate is described. The reaction features high functional group compatibility in air under solvent-free conditions without any additive and only water as the nontoxic byproduct, providing a strategy for the facile, economical, and eco-friendly construction of multiaryl-substituted pyridines from simple and readily available reactants.
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