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- W3085165578 abstract "Abstract Quercetin and quercetin derivatives are strong flavonoid antioxidants. Electrochemical oxidation of quercetin in the presence of 1,2,3,4-di-O-diisopropylidene-α- d -galactopyranose in acetonitrile has been studied using controlled-potential electrolysis, cyclic voltammetry and spectroscopy (UV–vis and LCMS). The results indicate that quercetin undergoes electrooxidation forming 2-(3,4-dihydroxybenzoyl)-2,4,6-trihydroxy-3(2H) benzofuranone and monoglycoconjugate of benzofuranone, subsequently." @default.
- W3085165578 created "2020-09-21" @default.
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- W3085165578 date "2020-12-01" @default.
- W3085165578 modified "2023-10-17" @default.
- W3085165578 title "Electrochemical study of quercetin in the presence of galactopyranose: Potential application to the electrosynthesis of glycoconjugates of quinone/quinone methide of quercetin" @default.
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- W3085165578 doi "https://doi.org/10.1016/j.jelechem.2020.114675" @default.
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