Synthetic study demonstrates bismuth(III)-catalyzed three-component selenation of imidazopyridines and arenes, highlighting an environmentally benign alternative to transition-metal catalysis.
Unsymmetrical diaryl selenides bearing heteroaromatic moieties have attracted increasing attention because of their notable biological activities. In this paper, a novel bismuth-catalyzed three-component reaction is reported for the synthesis of 3-selanylimidazopyridines from imidazopyridines, arylboronic acids, and elemental selenium. The reaction proceeded under aerobic conditions at 100 °C using BiI 3 (10 mol %) as the catalyst, affording the desired products in moderate to good yields. The application of this method to other electron-rich arenes was also explored. This transformation represents the first example of a three-component reaction catalyzed by a bismuth reagent. The use of BiI 3 , a non-hygroscopic and low-toxicity catalyst, offers an alternative to traditional transition-metal-catalyzed systems.
No takes yet. Share an insight, caveat, or question.
Aiba et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: