In this paper we report a [2 + 2] cycloaddition reaction between ketenes and benzils, characterized by an unusual double photochemical activation triggered by visible light. Employment of a flow system and optimization of reaction conditions through Design of Experiments resulted in moderate to good yields of the corresponding β-lactones. A thorough computational analysis allowed to elucidate the mechanism of the reaction and justify the observed diastereoselectivity. The reaction was also successfully tested with mixed benzils, showing complete regioselectivity. Graphical abstract: (Figure presented.).
CITATION STYLE
Minuto, F., Farinini, E., De Negri, S., Leardi, R., Ravelli, D., Solokha, P., & Basso, A. (2024). Two photons are better than one: continuous flow synthesis of ꞵ-lactones through a doubly photochemically-activated Paternò-Büchi reaction. Journal of Flow Chemistry, 14(1), 149–159. https://doi.org/10.1007/s41981-023-00297-7
Mendeley helps you to discover research relevant for your work.