In recent years, visible-light-induced transformations have taken a central role in driving forward the progress of modern organic synthesis. Despite the abundance of synthetic strategies enabling access to aryl- and alkyl-centered radicals, the exploitation of photochemistry to generate highly reactive alkenyl radicals has remained notably underdeveloped. Herein, we report a sustainable strategy for generating alkenyl radicals based on a photocatalytic single-electron transfer process. Through systematic optimization of conditions such as photocatalysts, light sources, and additives, we confirmed that radical reactions can efficiently occur under metal-free conditions using styrenylthiophene salt as radical donors, thiuram derivatives as radical acceptors, and 4CzIPN (1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene) as the photocatalyst. This method is operationally simple, environmentally friendly, and does not require the addition of precious metal reagents, providing a novel strategy for the methodology of alkenyl radical generation.
Bai-Xi et al. (Thu,) studied this question.