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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">From Chemistry Towards Technology Step-By-Step</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">From Chemistry Towards Technology Step-By-Step</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>От химии к технологии шаг за шагом</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="online">2782-1900</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">82272</article-id>
   <article-id pub-id-type="doi">10.52957/27821900_2022_03_106</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>Научные статьи</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>Scientific articles</subject>
    </subj-group>
    <subj-group>
     <subject>Научные статьи</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">Synthesis of pyridine- and piperidine-containing polycyclic compounds based on 2,6-dinitrohalogenbenzenes</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Synthesis of pyridine- and piperidine-containing polycyclic compounds based on 2,6-dinitrohalogenbenzenes</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Мохова</surname>
       <given-names>Любовь Андреевна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Mokhova</surname>
       <given-names>Lyubov Andreevna</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Соколов</surname>
       <given-names>Александр Андреевич</given-names>
      </name>
      <name xml:lang="en">
       <surname>Sokolov</surname>
       <given-names>Aleksandr Andreevich</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-2"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">Ярославский государственный университет им. П.Г. Демидова</institution>
    </aff>
    <aff>
     <institution xml:lang="en">P.G. Demidov Yaroslavl State University</institution>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-2">
    <aff>
     <institution xml:lang="ru">Ярославский государственный технический университет</institution>
    </aff>
    <aff>
     <institution xml:lang="en">Yaroslavl State Technical University</institution>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2022-09-23T00:00:00+03:00">
    <day>23</day>
    <month>09</month>
    <year>2022</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2022-09-23T00:00:00+03:00">
    <day>23</day>
    <month>09</month>
    <year>2022</year>
   </pub-date>
   <volume>3</volume>
   <issue>3</issue>
   <fpage>106</fpage>
   <lpage>115</lpage>
   <history>
    <date date-type="received" iso-8601-date="2022-09-01T00:00:00+03:00">
     <day>01</day>
     <month>09</month>
     <year>2022</year>
    </date>
    <date date-type="accepted" iso-8601-date="2022-09-19T00:00:00+03:00">
     <day>19</day>
     <month>09</month>
     <year>2022</year>
    </date>
   </history>
   <self-uri xlink:href="https://chemintech.ru/en/nauka/article/82272/view">https://chemintech.ru/en/nauka/article/82272/view</self-uri>
   <abstract xml:lang="ru">
    <p>This article deals with the study of the nitration of &#13;
4-chloro-3-nitrobenzoic acid. The substrate is highly deactivated for SEAr reactions and therefore strict conditions are required (anhydrous KNO3 in concentrated H2SO4 at 165 °C for 10 hours). We have developed methods for the transformation of 4-chloro-3,5-dinitrobenzoic acid and its ester into new polycyclic systems containing pyridine or piperidine fragments by quaternization and reduction reactions.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>This article deals with the study of the nitration of &#13;
4-chloro-3-nitrobenzoic acid. The substrate is highly deactivated for SEAr reactions and therefore strict conditions are required (anhydrous KNO3 in concentrated H2SO4 at 165 °C for 10 hours). We have developed methods for the transformation of 4-chloro-3,5-dinitrobenzoic acid and its ester into new polycyclic systems containing pyridine or piperidine fragments by quaternization and reduction reactions.</p>
   </trans-abstract>
   <kwd-group xml:lang="en">
    <kwd>4-chloro-3-nitrobenzoic acid</kwd>
    <kwd>N-(2</kwd>
    <kwd>6-dinitroaryl)pyridinium salts</kwd>
    <kwd>N-(2</kwd>
    <kwd>6-dinitroaryl)piperidines</kwd>
    <kwd>nitration</kwd>
    <kwd>pyridine quaternisation</kwd>
   </kwd-group>
   <funding-group>
    <funding-statement xml:lang="en">This work was carried out with the financial support of grant No MK-3459.2022.1.3 from the President of the Russian Federation for state support of young Russian scientists - can-didates of science.</funding-statement>
   </funding-group>
  </article-meta>
 </front>
 <body>
  <p></p>
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