“…Several catalyzed reactions were published for the synthesis of 1,2,4,5-tetra-substituted imidazoles using catalysts such as Y(NO 3 [100], bioglycerol-based recyclable carbon catalyst [102], Amberlyst A-15 [110], SBA-15/TFE (SBA-15/2,2,2-trifluoroethanol) [112], SBA-Pr-SO 3 H [113], silicasupported tin oxide nanoparticles [114], magnetic Fe 3 O 4 nanoparticles [119], L-proline [121], p-toluene sulfonic acid (PTSA) [126], solvent-free conditions with sodium dihydrogen phosphate [128], microwave irradiation [141][142][143], FeCl 3 ·6H 2 O [178], fluoroboric acid adsorbed on silica-gel (HBF 4 -SiO 2 ) [179], NHC (N -Heterocyclic Carbene) [180], trifluoroacetic acid [181], a novel organometallic catalyst (PSNP-CA) [182], MCM-41 [183], nano-TiCl 4 ·SiO 2 [184], and clay-supported titanium catalyst [185]. Highly substituted imidazole derivatives can be created using a new four-component and three-step reaction from alkoxyallenes, amines, iodine and nitriles with excellent yields.…”