Journal of the American Chemical Society · 2014 · 339 citations · 59 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryCoordination ChemistryEnzyme InhibitionHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisAmide Bond FormationHeterocycle FunctionalizationMedicinal Heterocycles
A Cu(OAc)2-mediated C-H amidation and amination of arenes and heteroarenes has been developed using a readily removable directing group. A wide range of sulfonamides, amides, and anilines function as amine donors in this reaction. Heterocycles present in both reactants are tolerated, making this a broadly applicable method for the synthesis of a family of inhibitors including 2-benzamidobenzoic acids and N-phenylaminobenzoates.
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