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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Dzhemileva, L.U.</author>
     <author>D'yakonov, V.A.</author>
     <author>Makarov, A.A.</author>
     <author>Andreev, E.N.</author>
     <author>Yunusbaeva, M.M.</author>
     <author>Dzhemilev, U.M.</author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2017</year>
    <pub-dates>
     <date>2018-01-24</date>
    </pub-dates>
   </dates>
   <doi>10.1039/C6OB02346K</doi>
   <abstract>The communication reports a new stereoselective method for the synthesis of a natural acetylenic alcohol, lembehyne B. The key stage of the process uses new cross-cyclomagnesiation reaction of aliphatic and oxygenated 1,2-dienes with Grignard reagents in the presence of a catalytic amount of Cp2TiCl2. A study of the cytotoxic properties of lembehyne B on tumor cell lines using flow cytometry demonstrated that this is a selective inducer of early apoptosis of the Jurkat, HL-60 and K562 cell cultures and hypodiploid (sub-G1) sub-population inducer in cell cycle studies for all cell lines used.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/941</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/1068</url>
    </pdf-urls>
   </urls>
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