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

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 r...

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Detalles Bibliográficos
Autores principales: Hou, Huiqing, Ma, Xinhua, Lin, Yingying, Lin, Jin, Sun, Weiming, Wang, Lei, Xu, Xiuzhi, Ke, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033184/
https://www.ncbi.nlm.nih.gov/pubmed/35480173
http://dx.doi.org/10.1039/d1ra02706a
Descripción
Sumario: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.