Answers are grounded in this paper and cite their sources.
Oxidative condensation-cyclization of aldehydes and aryl-2-pyridylmethylamines proceeded in the presence of a stoichiometric amount of elemental sulfur as an oxidant in the absence of catalyst. The reaction gave a variety of 1,3-diarylated imidazo[1,5-a]pyridines in good to high yields. The products showed fluorescence emission in a wavelength range of 454-524 nm. The quantum yields of 1,3-diarylated imidazopyridines were greatly improved compared to those of the parent 3-monosubstituted compounds.
No takes yet. Share an insight, caveat, or question.
Shibahara et al. (2009) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: