Tiny water droplets transmutate aniline into pyridine in ambient and catalyst-free conditions

Aniline can now be transformed into pyridine without adding any catalysts, oxidants or toxic reagents. In a recent study published in the Journal of the American Chemical Society, researchers achieved skeletal editing, involving the reorganization of the carbon-nitrogen bonds within an aromatic ring, by turning an aqueous solution of aniline into a mist of microdroplets.