Abstract
The possibility of synthesis of conjugates differing in molecular weight, degree of substitution of the dextran glycoside units, and, accordingly, in the solubility in water from a hydrophilic polymer (dextran) and an azlactone derivative of a sterically hindered phenol, 4-(4-hydroxy-3,5-di-tert-butylbenzylidene)-2-phenyl-4,5-dihydrooxazol-5-one, was analyzed, and their antiradical and antioxidative activity was studied.
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Translated from Zhurnal Prikladnoi Khimii, Vol. 78, No. 6, 2005, pp. 962–965.
Original Russian Text Copyright © 2005 by Sergeeva, Aref’ev, Domnina, Komarova.
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Sergeeva, O.Y., Aref’ev, D.V., Domnina, N.S. et al. Synthesis and Antioxidative Properties of Conjugates of Dextran with 4-(4-Hydroxy-3,5-di-tert-butylbenzylidene)-2-phenyl-4, 5-dihydrooxazol-5-one. Russ J Appl Chem 78, 940–943 (2005). https://doi.org/10.1007/s11167-005-0424-7
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DOI: https://doi.org/10.1007/s11167-005-0424-7