Journal of the American Chemical Society · 2008 · 235 citations · 24 references
PharmacyChemistryMedicinal ChemistryCatalysisSynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryMacrocycle SynthesisAnnulation ReactionsAza-diels-alder ReactionAzepine ChemistryAzide Functionalization
A convenient gold(III)-catalyzed synthesis of azepines from the intermolecular annulation of propargyl esters and alpha,beta-unsaturated imines is reported (19 examples, 55-95% yield). This formal [4 + 3]-cycloaddition reaction is proposed to proceed via a stepwise process involving intramolecular trapping of an allyl-gold intermediate.
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