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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Salimova, E.V.</author>
     <author>Mamaev, A.G.</author>
     <author>Tret'yakova, E. V.</author>
     <author>Kukovinets, O. S.</author>
     <author>Mavzyutov, A. R.</author>
     <author>Shvets, K. Yu.</author>
     <author>Parfenova, L. V.</author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2018</year>
    <pub-dates>
     <date>2019-02-08</date>
    </pub-dates>
   </dates>
   <doi>10.1134/S1070428018090245</doi>
   <abstract>3,11-Dihydroxy and 3,11-dioxo triterpenoids of the fusidane series reacted with acrylonitrile in 1,4-dioxane in the presence of alkali and phase-transfer catalyst to give mono- and bis(2-cyanoethoxy) and 2-cyanoethyl derivatives. The reaction with 3,11-dioxo analog afforded 2,2-disubstituted derivative as a result of addition of two cyanoethyl groups to the -position with respect to the C-3=O carbonyl group. The isolated compounds were screened for antibacterial and antifungal activities.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/908</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/1032</url>
    </pdf-urls>
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