<?xml version="1.0" encoding="UTF-8"?>
<xml>
 <records>
  <record>
   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Karimova, E.R.</author>
     <author>Baltina, L.A.</author>
     <author>Spirikhin, L.V.</author>
     <author>Kondratenko, R.M.</author>
     <author>Farkhutdinov, R.R.</author>
     <author>Petrova, I.V.</author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2015</year>
    <pub-dates>
     <date>2018-02-27</date>
    </pub-dates>
   </dates>
   <abstract>Quercetin (Q) methyl ethers were synthesized from CH3I under various conditions. The principal products from the reactions of Q with alkylhalides (CH3I, C4H9Br) in DMF were 3,7,4′-tri-O-alkyl ethers. The structures of the products were confirmed by PMR and 13C NMR spectra. The antioxidant activity of Q tetra- and tri-O-methyl ethers was demonstrated by chemiluminescence in model systems generating active oxygen species and promoting lipid peroxidation.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/680</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/774</url>
    </pdf-urls>
   </urls>
  </record>
 </records>
</xml>
