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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">actabiomedica</journal-id><journal-title-group><journal-title xml:lang="ru">Acta Biomedica Scientifica</journal-title><trans-title-group xml:lang="en"><trans-title>Acta Biomedica Scientifica</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2541-9420</issn><issn pub-type="epub">2587-9596</issn><publisher><publisher-name>Scientific Centre for Family Health and Human Reproduction Problems</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">actabiomedica-829</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ЭКСПЕРИМЕНТАЛЬНЫЕ ИССЛЕДОВАНИЯ В БИОЛОГИИ И МЕДИЦИНЕ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>EXPERIMENTAL RESEARCHES IN BIOLOGY AND MEDICINE</subject></subj-group></article-categories><title-group><article-title>СИНТЕЗ НОВЫХ НЕНАСЫЩЕННЫХ ТЕЛЛУРОРГАНИЧЕСКИХ СОЕДИНЕНИЙ С ПОТЕНЦИАЛЬНОЙ БИОЛОГИЧЕСКОЙ АКТИВНОСТЬЮ</article-title><trans-title-group xml:lang="en"><trans-title>SYNTHESIS OF NOVEL UNSATURATED ORGANOTELLURIUM COMPOUNDS WITH POTENTIAL BIOLOGICAL ACTIVITY</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мусалова</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Musalova</surname><given-names>M. V.</given-names></name></name-alternatives><email xlink:type="simple">maria_musalova@irioch.irk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Потапов</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Potapov</surname><given-names>V. A.</given-names></name></name-alternatives><email xlink:type="simple">v_a_potapov@irioch.irk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Амосова</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Amosova</surname><given-names>S. V.</given-names></name></name-alternatives><email xlink:type="simple">amosova@irioch.irk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Иркутский институт химии имени А.Е. Фаворского СО РАН</institution></aff><aff xml:lang="en"><institution>A.E. Favorsky Irkutsk Institute of Chemistry SB RAS, Irkutsk</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>28</day><month>04</month><year>2012</year></pub-date><volume>0</volume><issue>2(2)</issue><fpage>117</fpage><lpage>120</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Мусалова М.В., Потапов В.А., Амосова С.В., 2012</copyright-statement><copyright-year>2012</copyright-year><copyright-holder xml:lang="ru">Мусалова М.В., Потапов В.А., Амосова С.В.</copyright-holder><copyright-holder xml:lang="en">Musalova M.V., Potapov V.A., Amosova S.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.actabiomedica.ru/jour/article/view/829">https://www.actabiomedica.ru/jour/article/view/829</self-uri><abstract><p>На основе ацетиленов и тетрагалогенидов теллура разработаны эффективные синтетические подходы, к новым, потенциально биологически активным, теллурорганическим соединениям.</p></abstract><trans-abstract xml:lang="en"><p>Efficient synthetic approaches to novel organotellurium. compounds with potential biologically activity were elaborated, based, on acetylenes and tellurium, tetrahalid.es.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>биологическая активность</kwd><kwd>теллурорганические соединения</kwd><kwd>тетрагалогениды теллура</kwd><kwd>ацетилены</kwd></kwd-group><kwd-group xml:lang="en"><kwd>biological activity</kwd><kwd>organotellurium compounds</kwd><kwd>tellurium tetrahalides</kwd><kwd>acetylenes</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Потапов В.А., Мусалова М.В., Амосова С.В. 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