Publication | Closed Access
Synthesis of Imidazo[1,2-a]pyridines from Pyridines and p-Bromophenacyl Bromide O-Methyloxime
30
Citations
0
References
1996
Year
HeterocyclicBiochemistryNatural SciencesUndergo CyclizationOrganic ChemistryChemistryP-bromophenacyl Bromide O-methyloximeHeterocycle ChemistryHalogenationCorresponding Pyridinium SaltsSynthetic ChemistryEnantioselective SynthesisO-methyloxime Reacts
p-Bromophenacyl bromide O-methyloxime reacts with pyridines in acetone to form the corresponding pyridinium salts which, when heated in methanol in the presence of Et3N, undergo cyclization followed by elimination of MeOH to give imidazo[1,2-a]pyridines.