“…Enaminones combine ambident nucleophilicity of enamine and the ambident electrophilicity of enone to behave as versatile building blocks and synthetic intermediates in heterocycle synthesis . Our group have recently developed some efficient methods for the preparation of heterocycles, such as 1,2,3‐triazoles, pyrroles, pyridines, benzo[ b ][1,4] oxazepines, quinoxalines, N‐( 2‐pyridyl)pyrroles and benzo[ b ][1,4]oxazins based on enaminones under transition metal free conditions. In our continuing efforts in enaminone chemistry, herein we report a novel protocol to 2,4,6‐triarylpyridines from easily accessible N‐ enaminones and chalcones under base conditions (Scheme ).…”