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Electrochemical synthesis of quinazolinone via I 2 -catalyzed tandem oxidation in aqueous solution.

Huiqing HouXinhua MaYingying LinJin LinWeiming SunLei WangXiuzhi XuFang Ke
Published in: RSC advances (2021)
The development of protocols for synthesizing quinazolinones using biocompatible catalysts in aqueous medium will help to resolve the difficulties of using green and sustainable chemistry for their synthesis. Herein, using I 2 in coordination with electrochemical synthesis induced a C-H oxidation reaction which is reported when using water as the environmentally friendly solvent to access a broad range of quinazolinones at room temperature. The reaction mechanism strongly showed that I 2 cooperates electrochemically promoted the oxidation of alcohols, then effectively cyclizing amides to various quinazolinones.
Keyphrases
  • ionic liquid
  • room temperature
  • electron transfer
  • aqueous solution
  • hydrogen peroxide
  • gold nanoparticles
  • diabetic rats
  • high resolution
  • mass spectrometry
  • transition metal