Synthetic Communications · 2006 · 161 citations · 15 references
Natural SciencesChemistryMedicinal ChemistryCarbohydrate ChemistryCatalysisOrganic ChemistryCarbohydrate SynthesisCatalyst SynthesisHeterocycle SynthesisOrganic SynthesisImidazole ChemistryImidazole SynthesisRoom-temperature SynthesisTriazole Synthesis
Abstract A general protocol has been developed for the rapid synthesis of 2,4,5‐trisubstituted and 1,2,4,5‐tetrasubstituted imidazoles in high yields using ZrCl4 as an efficient catalyst at room temperature. A variety of aromatic, aliphatic, and terpenoidal aldehydes underwent condensation with NH4OAc/amines to give the imidazoles. Similarly, the imidazole glycoconjugates are prepared in good yields from the corresponding glycosyl aldehydes.
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