Microdroplet chemistry enables catalyst-free skeletal editing

A diagram showing aniline going through heterocyclic transmutation via a droplet of water to form pyridine

Source: © Abhijit Nandy et al, J. Am. Chem. Soc. 2026

Hydroxyl radicals power transformation of aniline into pyridine

Water microdroplets are the latest addition to the skeletal editing toolbox. Powered by nothing more than a fine spray of water, researchers in India achieved a complex ring rearrangement with important implications for drug design and synthesis – the conversion of aniline to pyridine. The reagent-free process provides crucial insight into the fundamental mechanism of microdroplets’ unique reactivity and potentially opens the door to the green synthesis of other valuable heterocycles in future.