Photocatalytic remote alkenylation of hydroxamides with enamides: synthesis of trisubstituted enamides <i>via</i> a radical pathway

A photocatalytic radical-mediated strategy has been developed for the 1,5-hydrogen atom transfer (1,5-HAT)/alkenylation of hydroxamides with enamides, enabling the efficient synthesis of diverse, previously unreported trisubstituted enamides in moderate to good yields under mild conditions. This <i>N</i>-centered radical-triggered γ-C(sp³)-H alkenylation reaction demonstrates broad substrate scope, excellent functional group tolerance, and remarkable regio- and stereoselectivity. The proposed mechanism involves a sequential cascade of single-electron transfer (SET), 1,5-HAT, radical addition, oxidation, and deprotonation.