Visible-light-induced Reactions Driven by Photochemical Activity of Quinolinone and Coumarin Scaffolds

Organic photocatalysis has garnered significant interest in the field of photochemistry because of its ability to generate active radical species under mild conditions via energy or electron transfer from the excited state of photosensitizers to organic molecules. Quinolinones and coumarins are privileged scaffolds that are widely distributed in natural products and pharmaceutical agents. Recently, quinolinones and coumarins have emerged as promising organic photosensitizers for a variety of chemical transformations. Significant advances in the development of synthetic methods via organic photocatalysis have elucidated their essential electronic properties, leading to the development of highly site-selective synthetic methods. This mini-review highlights recent innovative approaches to site-selective C-H bond functionalization catalyzed by light-absorbing quinolinone and coumarin scaffolds.

Automated summary

Organic photocatalysis has gained attention for generating active radical species under mild conditions. Quinolinones and coumarins are widely distributed and promising organic photosensitizers, leading to the development of highly site-selective synthetic methods. Innovative approaches using light-absorbing quinolinone and coumarin scaffolds have been highlighted for site-selective C-H bond functionalization.