The Journal of Organic Chemistry · 2016 · 20 citations · 31 references
Natural SciencesChemistryCatalysisGreen ChemistryOrganic ChemistryCarboxylic AcidsCarboxylic DerivativesHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisAcid ChloridesCarboxylic Acid Derivative SynthesisCarboxylic Acid SynthesisFunctional Group ToleranceHeterocycle FunctionalizationKetonesMild Reaction ConditionsSubstrate Scope
A practical and highly effective one-pot synthesis of versatile heteroaryl ketones directly from carboxylic acids and heteroaryl halides under mild conditions is reported. This method does not require derivatization of carboxylic acids (preparation of acid chlorides, Weinreb amides, etc.) or the use of any additives/catalysts. A wide substrate scope of carboxylic acids with high functional group tolerance has also been demonstrated. The results reveal that the presence of an α-nitrogen on the halide substrate greatly improves the desired ketone formation.
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J. Scott Sawyer, Douglas W. Beight, Karen S. Britt et al. · Bioorganic & Medicinal Chemistry Letters · 2004 · 163 citations
New Syntheses of Substituted Pyridines via Bromine–Magnesium Exchange
François Trécourt, Gilles Breton, Véronique Bonnet et al. · Tetrahedron · 2000 · 131 citations