Abstract
Abstract The potentially bioactive 2-aryl-thiazolo[4,5- b ]pyridines were synthesized via palladium-catalyzed desulfitative cross-coupling reaction between multisubstituted thiazolo[4,5- b ]pyridine thioethers and boronic acids. Yields of 48%–94% were obtained with copper(I) thiophene-2-carboxylate in the system.
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