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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">vestich</journal-id><journal-title-group><journal-title xml:lang="ru">Известия Национальной академии наук Беларуси. Серия химических наук</journal-title><trans-title-group xml:lang="en"><trans-title>Proceedings of the National Academy of Sciences of Belarus, Chemical Series</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1561-8331</issn><issn pub-type="epub">2524-2342</issn><publisher><publisher-name>The Republican Unitary Enterprise Publishing House "Belaruskaya Navuka"</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">vestich-295</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>ОБЗОРЫ</subject></subj-group></article-categories><title-group><article-title>ГЕТЕРОЦИКЛИЧЕСКИЕ ПРОИЗВОДНЫЕ МЕТАЛЛОЦЕНОВ</article-title><trans-title-group xml:lang="en"><trans-title>HETEROCYCLES DERIVATIVES OF METALLOCENES</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>Колесник</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kolesnik</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>мл. науч. сотрудник</p><p>ул. Сурганова, 13, 220072</p></bio><bio xml:lang="en"><p>Junior Researcher</p><p>13, Surganov Str., 220072</p></bio><email xlink:type="simple">zvetok_kaktusa@mail.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>Дикусар</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Dikusar</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. хим. наук, ст. науч. сотрудник</p><p>ул. Сурганова, 13, 220072</p></bio><bio xml:lang="en"><p>Ph. D. (Chemistry), Senior Researcher</p><p>13, Surganov Str., 220072</p></bio><email xlink:type="simple">dikusar@ifoch.bas-net.by</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт физико-органической химии НАН Беларуси, Минск</institution></aff><aff xml:lang="en"><institution>Institute of Physical Organic Chemistry of the National Academy of Sciences of Belarus, Minsk</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>14</day><month>12</month><year>2017</year></pub-date><volume>0</volume><issue>4</issue><fpage>107</fpage><lpage>125</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Колесник И.А., Дикусар Е.А., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Колесник И.А., Дикусар Е.А.</copyright-holder><copyright-holder xml:lang="en">Kolesnik I.A., Dikusar E.A.</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://vestichem.belnauka.by/jour/article/view/295">https://vestichem.belnauka.by/jour/article/view/295</self-uri><abstract><p>Обзор посвящен методологии получения производных металлоценов, содержащих гетероциклические фрагменты, что позволяет не только усилить специфическое действие и свойства последних, но и получать соединения с принципиально новыми свойствами. Изоксазол входит в состав множества природных биологически активных соединений, его производные используются для лечения заболеваний центральной нервной системы, как противоопухолевые агенты, анальгетики, анестетики, миорелаксанты, антибиотики. Целенаправленно синтезированные производные изотиазола проявляют противовирусную, противораковую, антибиотическую активность, являются эффективными иммунодепрессантами, противовоспалительными и противотромбозными средствами. Производные указанных азолов занимают особое место в агрохимии в качестве гербицидов, пестицидов, инсектицидов или фунгицидов. В свою очередь соединения ферроцена представляют интерес ввиду широкого спектра их химических превращений и разнообразных путей практического использования в технике, электрохимии, катализе, а также в биологии и медицине. Более того, отмечено, что включение ферроценового фрагмента в органическую молекулу зачастую приводит к возникновению совершенно новых свойств и в том числе – биологической активности. Это обусловлено увеличением скорости проникновения вещества через клеточные мембраны из-за высокой липофильности ферроценового фрагмента, а следовательно, протеканием аномального метаболизма ферроценсодержащего соединения. Не менее разнообразны и направления применения цимантреновых производных; однако использование биологически активных соединений на его основе ограничено по причине достаточно высокой токсичности цимантренового фрагмента. Большой интерес представляет способность цимантреновой структуры к переметаллированию с образованием производных других металлоценов. </p></abstract><trans-abstract xml:lang="en"><p>The review article is devoted to the methodology of getting derivatives containing metallocene and heterocyclic fragments united in one molecule, which allows not only strengthening the specific action and the properties of the latter, but also obtaining compounds with radically new properties. Isoxazole is a part of many biologically active compounds, and its derivatives are used to treat diseases of the central nervous system, such as anti-tumor agents, analgesics, anesthetics, muscle relaxants, antibiotics. Purposefully synthesized isothiazole derivatives exhibit antiviral, anticancer, antibiotic activity, are effective immunosuppressive drugs, anti-inflammatory and antithrombotic agents. Derivatives of these azoles have a special place in agrochemicals as herbicides, pesticides, insecticides or fungicides. In turn, ferrocene compounds are of interest due to their wide range of chemical transformations and various ways of practical use in the art of electrochemistry, catalysis, and also in medicine and biology. Moreover, it is noted that the inclusion of the ferrocene moiety in an organic molecule often leads to completely new properties, including biological activity. This is due to the increase of penetration rate of material through the cell membranes due to the high lipophilicity of the ferrocene moiety, and therefore, the occurrence of abnormal metabolism ferrocene compound. Cymantrene derivatives applications are no less diverse; however, the use of biologically active compounds based on it is limited because of quite high toxicity of cymantrene fragment. Of great interest is the ability of the cymantrene structure to transmetallation with the formation of derivatives of other metallocenes. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>ферроцен</kwd><kwd>цимантрен</kwd><kwd>халкон</kwd><kwd>дихалкон</kwd><kwd>изотиазол</kwd><kwd>изоксазол</kwd><kwd>циклизация</kwd><kwd>гетероцикли-ческие соединения</kwd></kwd-group><kwd-group xml:lang="en"><kwd>ferrocene</kwd><kwd>cymantrene</kwd><kwd>chalcone</kwd><kwd>dichalcone</kwd><kwd>isothiazole</kwd><kwd>isoxazole</kwd><kwd>cyclization</kwd><kwd>heterocyclic compounds</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена при финансовой поддержке Белорусского республиканского фонда фундаментальных исследований (гранты Х 15СО-006, Х 15 М-029) и Сибирского Отделения Российской академии наук (грант СО РАН № 4).</funding-statement><funding-statement xml:lang="en">This work has been performed with a financial support of Belarusian Republican Foundation for Fundamental Research (grants № Х 15СО-006 and Х 15 М-029) and Siberian Branch of the Russian Academy of Sciences (grant СО РАН № 4).</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Машковский, М. 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