The Journal of Organic Chemistry · 2019 · 12 citations · 60 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryDiversity-oriented SynthesisHeterocycle SynthesisOrganic SynthesisRetrosynthetic AnalysisAldehydesBenzimidazole ChemistryBenzimidazole SynthesisImidazole ChemistryPyridine Synthesis
An unprecedented one-pot successive base-mediated allylic amination/cycloisomerization reaction strategy has been developed to construct diversely substituted imidazo[1,2-a]pyridines and benzimidazo[1,2-a]pyridines in good to excellent yield. The advantage of this unique [4 + 2]-annulation lies in the employment of readily accessible starting materials, Morita–Baylis–Hillman acetates of acetylenic aldehydes as C4 synthons, and simple imidazoles or benzimidazoles as C2 synthons.
60
Chafiq Hamdouchi, Jesús de Blas, Mirian del Prado et al. · Journal of Medicinal Chemistry · 1998 · 279 citations