Dynamic Kinetic Sensitization of β-Dicarbonyl Compounds-Access to Medium-Sized Rings by De Mayo-Type Ring Expansion

Herein, we present a photocatalyzed two-carbon ring expansion of beta-dicarbonyl compounds with unactivated olefins that provides facile access to medium-sized rings. Selective sensitization of the substoichiometric enol tautomer enables reactivity of substrates incompatible with the classical De Mayo reaction conditions. Key to success is the identification of the metal-based sensitizer fac-[Ir(CF3-pmb)(3)], which can be excited using common near-visible LEDs, and possesses a high triplet excited state energy of 73.3 kcal mol(-1). This exactly falls in the range between the triplet energies of the enol and keto tautomer, thereby enabling a dynamic kinetic sensitization. Demonstrating the applicability of fac-[Ir(CF3-pmb)(3)] as a photocatalyst in organic synthesis for the first time, we describe a two-step photocycloaddition-ring-opening cascade with beta-ketoesters, -diketones, and -ketoamides. The mechanism has been corroborated by time-resolved spectroscopy, as well as further experimental and computational studies.

Automated summary

In this research, a photocatalyzed two-carbon ring expansion of beta-dicarbonyl compounds with unactivated olefins was achieved, facilitated by selective sensitization of the substoichiometric enol tautomer and the identification of a metal-based sensitizer fac-[Ir(CF3-pmb)(3)]. This sensitizer proved effective in facilitating the reaction, allowing for the synthesis of medium-sized rings in organic compounds.