Sono‐Photoinduced Self‐Catalyzed Acyloxylation of 4H‐Pyrido[1,2‐a]Pyrimidin‐4‐Ones with Aryl Diacyl Peroxides and Bioactivities of Products

View at publisher
Authors: Ning-Bo Li, Yun‐Chang Liu, Yong‐Dong Wei, Di Zhang, Yao‐Dan Xu, Jun-Mei Peng, Jie Qiao, Wei‐Min He
Cited by: 1
References: 67

Abstract

A novel self‐catalyzed sono‐photoinduced C–H acyloxylation of 4H‐pyrido[1,2‐a]pyrimidin‐4‐ones with aryl diacyl peroxides has been established. This protocol employs eco‐friendly DMC as the solvent and proceeds efficiently without exogenous catalysts or additives, affording C3‐acyloxylated derivatives in good to excellent yields. The synergistic sono‐photocatalysis strategy significantly enhances reaction kinetics, product yields, and energy efficiency compared to traditional photocatalytic methods. Moreover, preliminary biological assays reveal that the synthesized compounds exhibit promising antitumor activities.

Fields of Study & Subjects

Radical Photochemical Reactions Catalytic C–H Functionalization Methods Oxidative Organic Chemistry Reactions

Publication details

Journal / source
Advanced Synthesis & Catalysis
Publisher
Wiley
Volume
368
Issue
9
Publication date
20 April 2026
Language
EN