Answers are grounded in this paper and cite their sources.
An efficient method for the synthesis of benzimidazo[1,2-a]quinolines under transition-metal-free conditions has been developed through a cascade reaction involving sequential aromatic nucleophilic substitution and intramolecular Knoevenagel condensation reactions. This method is applicable for the synthesis of a wide range of benzimidazo[1,2-a]quinoline derivatives from readily available 2-fluoroarylaldehyde and benzimidazole substrates.
No takes yet. Share an insight, caveat, or question.
Kato et al. (2013) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: