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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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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 |
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. |
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