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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Raskildinaa, G.Z.</author>
     <author>Valieva, V.F.</author>
     <author>Ozdena, I.V.</author>
     <author>Meshcheryakova, S.A.</author>
     <author>Spirikhin, L.V.</author>
     <author>Zlotskiia, S.S.</author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2017</year>
    <pub-dates>
     <date>2018-03-07</date>
    </pub-dates>
   </dates>
   <abstract>6-Methyluracil derivatives containing a gem-dichlorocyclopropane and a 1,3-dioxolane fragments&#13;
were synthesized for the first time. The condensation of 6-methyluracil with chloromethyl derivatives gives a&#13;
mixture of N1&#13;
- and N3&#13;
-monosubstituted products, and the profound N-alkylation of this compound provides&#13;
disubstituted uracils. The structure of the synthesized compounds was studied by H1&#13;
 and 13С NMR spectroscopy&#13;
and their relative antioxidant activity was evaluated by luminol-dependent chemiluminescence measurements.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/697</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/800</url>
    </pdf-urls>
   </urls>
  </record>
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