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Russian Journal of Applied Chemistry

, Volume 78, Issue 6, pp 940–943 | Cite as

Synthesis and Antioxidative Properties of Conjugates of Dextran with 4-(4-Hydroxy-3,5-di-tert-butylbenzylidene)-2-phenyl-4, 5-dihydrooxazol-5-one

  • O. Yu. Sergeeva
  • D. V. Aref’ev
  • N. S. Domnina
  • E. A. Komarova
Organic Synthesis and Industrial Organic Chemistry

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.

Keywords

Polymer Molecular Weight Phenol Glycoside Dextran 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© MAIK “Nauka/Interperiodica” 2005

Authors and Affiliations

  • O. Yu. Sergeeva
    • 1
  • D. V. Aref’ev
    • 1
  • N. S. Domnina
    • 1
  • E. A. Komarova
    • 1
  1. 1.St. Petersburg State UniversitySt. PetersburgRussia

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