Electrochemical oxidative selenylation of imidazo[1,2–a]pyridines with diselenides

Add time:09/01/2019    Source:sciencedirect.com

Electrochemical oxidative selenylation of imidazo[1,2–a]pyridines has been developed. The reaction proceeds in an undivided electrochemical cell equipped with glassy carbon electrodes employing LiClO4 as a supporting electrolyte. This approach is environmentally benign by using shelf-stable diselenides as selenium source and electrons as oxidizing reagents. The present protocol offers a facile way to prepare 3-selenylated imidazopyridine derivatives.

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