Reductive photoredox transformations of carbonyl derivatives enabled by strongly reducing photosensitizers

Abstract

photoinduced electron transfer. In this work, we unveil a range of photoredox transformations on ketones and imines, enabled by strongly reducing photosensitizers and operating under simple, general conditions with a single sacrificial reductant and no additives. Specific reactions described here are umpolung C-C bond forming reactions between aromatic ketones or imines and electron-poor alkenes, imino-pinacol homocoupling reactions of challenging alkyl-aryl imine substrates, and γ-lactonization reactions of aromatic ketones with methyl acrylate. The reactions are all initiated by photoinduced electron transfer to form a ketyl or iminyl that is subsequently trapped.

Topics & Concepts