Abstract
The oxidation of primary hydroxyl groups in dermatan sulfate with the NaOCl-NaBr-2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) reagent in an aqueous alkaline medium was carried out for the first time. Modified dermatan sulfates containing hydrated aldehyde (15–50%) and carboxyl (25–100%) groups were obtained.
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- DS:
-
dermatan sulfate
- IdoA:
-
iduronic acid
- TEMPO:
-
2,2,6,6-tetramethylpiperidine-1-oxyl
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Original Russian Text © I.Yu. Ponedel’kina, E.A. Khaibrahmanova, V.N. Odinokov, L.M. Khalilov, U.M. Dzhemilev, 2010, published in Bioorganicheskaya Khimiya, 2010, Vol. 36, No. 3, pp. 387–391.
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Ponedel’kina, I.Y., Khaibrahmanova, E.A., Odinokov, V.N. et al. Oxidation of dermatan sulfate with a NaOCl-NaBr-2,2,6,6-tetramethylpiperidine-1-oxyl reagent in an aqueous medium. Russ J Bioorg Chem 36, 354–358 (2010). https://doi.org/10.1134/S1068162010030106
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DOI: https://doi.org/10.1134/S1068162010030106


