Organic Letters · 2008 · 479 citations · 31 references
Natural SciencesChemistryMedicinal ChemistryCatalysisInorganic ChemistryOrganic ChemistryCatalytic MechanismsCross-coupling ReactionsHalogen ChemistryMicrowave-assisted SynthesisRadical ReactionsReaction MechanismsArylation ReactionsMicrowave Irradiation EffectsMicrowave-assisted CatalysisNitrogen HeterocyclesRadical MechanismsTransition Metal CatalysisTransition Metal CatalystsTransition-metal-catalyzed Heterocycle Synthesis
The biaryl coupling of electron-deficient nitrogen heterocycles and haloarenes can be promoted by potassium t-butoxide alone, without the addition of any exogenous transition metal species. Electron-deficient nitrogen heterocycles such as pyridine, pyridazine, pyrimidine, pyrazine, and quinoxaline are arylated with haloarenes. Control experiments support a radical-based mechanism. Taking these findings into account, radical processes may be partially involved in the reported transition-metal-catalyzed arylation reactions employing t-butoxide bases and haloarenes under elevated temperatures or under microwave irradiation.
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Catalytic Direct Arylation of Heteroaromatic Compounds
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Aromatic substitution by the SRN1 mechanism
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