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Synthesis of triphenylamine-imidazo[1,2-a]pyridine via Groebke-Blackburn-Bienaymé Reaction
2020
Proceedings of The 24th International Electronic Conference on Synthetic Organic Chemistry
unpublished
Preserved Fulltext
A series of triphenylamine-imidazo[1,2-a]pyridine were synthesized in moderate yields (57-67%) by Groebke-Blackburn-Bienaymé reaction (GBBR) under catalyst-and solvent green conditions. The molecules synthesized containing triphenylamine and imidazo[1,2-a]pyridines cores which are considered a privileged cores exhibited fluorescence and medicinal properties.
doi:10.3390/ecsoc-24-08422
fatcat:uzcvo6qkmbaebllqnlja352h2u