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- W2016290885 abstract "Sodium periodate oxidation of caffeic acid was investigated in aqueous solutions with pH ranging from 2 to 7. Products formed from quinone evolution were monitored by HPLC. It was found that they were affected both qualitatively and quantitatively by the conditions of the reaction. The rate and the yield of the reaction increased with the pH. In particular, two products obtained at pH values lower than 4.6 approximately, were analysed and isolated by reverse phase HPLC. By using 1H and 13C NMR and mass spectrometries, these compounds were shown to be two stereoisomers of 2,5-(3′,4′-dihydroxyphenyl)tetrahydrofuran 3,4-dicarboxylic acid." @default.
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- W2016290885 date "1994-01-01" @default.
- W2016290885 modified "2023-10-12" @default.
- W2016290885 title "Characterization of compounds obtained by chemical oxidation of caffeic acid in acidic conditions" @default.
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- W2016290885 doi "https://doi.org/10.1016/s0031-9422(00)94790-3" @default.
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