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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Baltina, L.A.</author>
     <author>Shabieva, E.R.</author>
     <author>Kondratenko, R.M.</author>
     <author>Spirikhin, L.V.</author>
     <author>Baltina, L.A.</author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2017</year>
    <pub-dates>
     <date>2018-01-31</date>
    </pub-dates>
   </dates>
   <doi>10.1007/s10600-017-2148-3</doi>
   <abstract>The reaction of paeoniflorin (PF) with refluxing MeOH in the presence of cation exchanger KU-2-8 (H+) formed a mixture of the 4-O-methyl- and 4-oxo-9-O-methyl ethers (1:1, overall yield 90%) that were separated by chromatography over silica gel. The reaction of PF with EtOH and BuOH under analogous conditions also formed mixtures of the ethyl and butyl ethers from which 4-oxo-9-O-ethyl(butyl) ethers were isolated as the tetra-O-acetates. The structures of the obtained compounds were confirmed using PMR and 13C NMR spectra.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/1128</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/1287</url>
    </pdf-urls>
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