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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">82367</article-id>
   <article-id pub-id-type="doi">10.52957/27821900_2022_02_79</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 substituted 1,3-dihydropyrrolo[3,4-F]indole-2,5,7-trions</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Synthesis of substituted 1,3-dihydropyrrolo[3,4-F]indole-2,5,7-trions</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Чиркова</surname>
       <given-names>Жанна Вячеславовна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Chirkova</surname>
       <given-names>Zhanna Vyacheslavovna</given-names>
      </name>
     </name-alternatives>
     <email>chirkovazhv@ystu.ru</email>
     <bio xml:lang="ru">
      <p>доктор химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>doctor of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Филимонов</surname>
       <given-names>Сергей Иванович</given-names>
      </name>
      <name xml:lang="en">
       <surname>Filimonov</surname>
       <given-names>Sergey Ivanovich</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>доктор химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>doctor of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Макарова</surname>
       <given-names>Елена Сергеевна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Makarova</surname>
       <given-names>Elena Sergeevna</given-names>
      </name>
     </name-alternatives>
     <email>makarovaes@ystu.ru</email>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Кабанова</surname>
       <given-names>Мария Валерьевна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Kabanova</surname>
       <given-names>Maria Valer'evna</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <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="2022-06-23T00:00:00+03:00">
    <day>23</day>
    <month>06</month>
    <year>2022</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2022-06-23T00:00:00+03:00">
    <day>23</day>
    <month>06</month>
    <year>2022</year>
   </pub-date>
   <volume>3</volume>
   <issue>2</issue>
   <fpage>79</fpage>
   <lpage>85</lpage>
   <history>
    <date date-type="received" iso-8601-date="2022-04-13T00:00:00+03:00">
     <day>13</day>
     <month>04</month>
     <year>2022</year>
    </date>
    <date date-type="accepted" iso-8601-date="2022-06-06T00:00:00+03:00">
     <day>06</day>
     <month>06</month>
     <year>2022</year>
    </date>
   </history>
   <self-uri xlink:href="https://chemintech.ru/en/nauka/article/82367/view">https://chemintech.ru/en/nauka/article/82367/view</self-uri>
   <abstract xml:lang="ru">
    <p>The paper concerns the development of the method for the preparation of functional isoindole-1,3-diones derivatives based on 5-nitro-4-phenacylphthalonitriles using Schmidt rearrangement.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>The paper concerns the development of the method for the preparation of functional isoindole-1,3-diones derivatives based on 5-nitro-4-phenacylphthalonitriles using Schmidt rearrangement.</p>
   </trans-abstract>
   <kwd-group xml:lang="en">
    <kwd>sodium azide</kwd>
    <kwd>5-nitro-4-phenacylphthalonitriles</kwd>
    <kwd>sulphuric acid</kwd>
    <kwd>Schmidt rearrangement</kwd>
    <kwd>isoindole-1</kwd>
    <kwd>3-diones</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
 </body>
 <back>
  <ref-list>
   <ref id="B1">
    <label>1.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Thigulla, Ya., Ranga, S., Ghosal, S., Subbalakshmi, J. &amp; Bhattacharya, A. (2017) One-Pot Two Step Nazarov-Schmidt Rearrangement for the Synthesis of Fused δ-Lactam Systems, Chem. Select, 2(30), pp. 9744-9750. DOI: 10.1002/slct.201701848 [online]. Available at: https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/slct.201701848 (accessed on 13.01.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Thigulla, Ya., Ranga, S., Ghosal, S., Subbalakshmi, J. &amp; Bhattacharya, A. (2017) One-Pot Two Step Nazarov-Schmidt Rearrangement for the Synthesis of Fused δ-Lactam Systems, Chem. Select, 2(30), pp. 9744-9750. DOI: 10.1002/slct.201701848 [online]. Available at: https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/slct.201701848 (accessed on 13.01.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B2">
    <label>2.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Bräse, S., Banert, K. (Eds.) (2010) Organic azides: syntheses and applications. John Wiley &amp; Sons. DOI: 10.1002/9780470682517 [online]. Available at: https://onlinelibrary.wiley.com/doi/10.1002/9780470682517.ch4 (accessed on 22.01.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Bräse, S., Banert, K. (Eds.) (2010) Organic azides: syntheses and applications. John Wiley &amp; Sons. DOI: 10.1002/9780470682517 [online]. Available at: https://onlinelibrary.wiley.com/doi/10.1002/9780470682517.ch4 (accessed on 22.01.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B3">
    <label>3.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Lang, S. &amp; Murphy, J.A. (2006) Azide rearrangements in electron-deficient systems, Chem. Soc. Rev., 35(2), pp. 146-156. DOI: 10.1039/B505080D [online]. Available at: https://pubs.rsc.org/en/content/articlelanding/2006/cs/b505080d/unauth (accessed on 16.02.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Lang, S. &amp; Murphy, J.A. (2006) Azide rearrangements in electron-deficient systems, Chem. Soc. Rev., 35(2), pp. 146-156. DOI: 10.1039/B505080D [online]. Available at: https://pubs.rsc.org/en/content/articlelanding/2006/cs/b505080d/unauth (accessed on 16.02.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B4">
    <label>4.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Ding, S. L., Ji, Y., Su, Y., Li, R. &amp; Gu, P. (2019) Schmidt Reaction of ω-Azido Valeryl Chlorides Followed by Intermolecular Trapping of the Rearrangement Ions: Synthesis of Assoanine and Related Pyrrolophenanthridine Alkaloids, J. Org. Chem., 84(4), pp. 2012-2021. DOI: 10.1021/acs.joc.8b03018 [online]. Available at: https://pubs.acs.org/doi/abs/10.1021/acs.joc.8b03018 (accessed on 03.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Ding, S. L., Ji, Y., Su, Y., Li, R. &amp; Gu, P. (2019) Schmidt Reaction of ω-Azido Valeryl Chlorides Followed by Intermolecular Trapping of the Rearrangement Ions: Synthesis of Assoanine and Related Pyrrolophenanthridine Alkaloids, J. Org. Chem., 84(4), pp. 2012-2021. DOI: 10.1021/acs.joc.8b03018 [online]. Available at: https://pubs.acs.org/doi/abs/10.1021/acs.joc.8b03018 (accessed on 03.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B5">
    <label>5.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Nyfeler, E. &amp; Renaud, Ph. (2006) Intramolecular Schmidt Reaction: Applications in Natural Product Synthesis, Chimia, 60(5), pp. 276-284. DOI: 10.2533/000942906777674714 [online]. Available at: https://chimia.ch/chimia/article/view/2006_276/3453 (accessed on 01.03.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Nyfeler, E. &amp; Renaud, Ph. (2006) Intramolecular Schmidt Reaction: Applications in Natural Product Synthesis, Chimia, 60(5), pp. 276-284. DOI: 10.2533/000942906777674714 [online]. Available at: https://chimia.ch/chimia/article/view/2006_276/3453 (accessed on 01.03.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B6">
    <label>6.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Zou, H., Zhou, L., Li, Y., Cui, Y., Zhong, H., Pan, Z., Yang, Zh. &amp; Quan, J. (2010) Benzo[e]isoindole-1,3-diones as potential inhibitors of glycogen synthase kinase-3 (GSK-3). Synthesis, kinase inhibitory activity, zebrafish phenotype, and modeling of binding mode, J. Med. Chem., 53(3), pp. 994-1003. DOI: 10.1021/jm9013373 [online]. Available at: https://pubs.acs.org/doi/abs/10.1021/jm9013373 (accessed on 03.02.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Zou, H., Zhou, L., Li, Y., Cui, Y., Zhong, H., Pan, Z., Yang, Zh. &amp; Quan, J. (2010) Benzo[e]isoindole-1,3-diones as potential inhibitors of glycogen synthase kinase-3 (GSK-3). Synthesis, kinase inhibitory activity, zebrafish phenotype, and modeling of binding mode, J. Med. Chem., 53(3), pp. 994-1003. DOI: 10.1021/jm9013373 [online]. Available at: https://pubs.acs.org/doi/abs/10.1021/jm9013373 (accessed on 03.02.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B7">
    <label>7.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Figg, W.D., Raje, S., Bauer, K.S., Tompkins, A., Venzon, D., Bergan, R., Chen, A., Hamilton, M., Pluda, J. &amp; Reed, E. (2000) Pharmacokinetics of thalidomide in an elderly prostate cancer population, J. Pharm. Sci., 88(1), pp. 121-125. DOI: 10.1021/js980172i [online]. Available at: https://onlinelibrary.wiley.com/doi/abs/10.1021/js980172i (accessed on 03.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Figg, W.D., Raje, S., Bauer, K.S., Tompkins, A., Venzon, D., Bergan, R., Chen, A., Hamilton, M., Pluda, J. &amp; Reed, E. (2000) Pharmacokinetics of thalidomide in an elderly prostate cancer population, J. Pharm. Sci., 88(1), pp. 121-125. DOI: 10.1021/js980172i [online]. Available at: https://onlinelibrary.wiley.com/doi/abs/10.1021/js980172i (accessed on 03.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B8">
    <label>8.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Ouenadio, F., Walchshofer, N., Trentesaux, C., Barret, R. &amp; Paris, J. (2001) Synthesis and antiproliferative activity of [2-(phthaloylamino)alkyl]triphenyl phosphonium derivatives against K562 cell line, Anti-Cancer Drugs, 12(7), pp. 603-606. DOI: 10.1097/00001813-200108000-00007 [online]. Available at: https://journals.lww.com/anti-cancerdrugs/Abstract/2001/08000/Synthesis_and_antiproliferative_activity_of.7.aspx (accessed on 13.02.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Ouenadio, F., Walchshofer, N., Trentesaux, C., Barret, R. &amp; Paris, J. (2001) Synthesis and antiproliferative activity of [2-(phthaloylamino)alkyl]triphenyl phosphonium derivatives against K562 cell line, Anti-Cancer Drugs, 12(7), pp. 603-606. DOI: 10.1097/00001813-200108000-00007 [online]. Available at: https://journals.lww.com/anti-cancerdrugs/Abstract/2001/08000/Synthesis_and_antiproliferative_activity_of.7.aspx (accessed on 13.02.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B9">
    <label>9.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Sansom, G.N., Kirk, N.S., Guise, C.P., Anderson, R.F., Smaill, J.B., Patterson, A.V. &amp; Kelso, M.J. (2019) Prototyping kinase inhibitor-cytotoxin anticancer mutual prodrugs activated by tumour hypoxia: A chemical proof of concept study, Bioorg Med. Chem. Lett., 29(10), pp. 1215-1219. DOI: 10.1016/j.bmcl.2019.03.015 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0960894X19301441 (accessed on 11.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Sansom, G.N., Kirk, N.S., Guise, C.P., Anderson, R.F., Smaill, J.B., Patterson, A.V. &amp; Kelso, M.J. (2019) Prototyping kinase inhibitor-cytotoxin anticancer mutual prodrugs activated by tumour hypoxia: A chemical proof of concept study, Bioorg Med. Chem. Lett., 29(10), pp. 1215-1219. DOI: 10.1016/j.bmcl.2019.03.015 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0960894X19301441 (accessed on 11.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B10">
    <label>10.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Lee, H.J., Lim, S.J., Oh, S.J., Moon, D.H., Kim, D.J., Tae, J. &amp; Yoo, K.H. (2008) Isoindol-1,3-dione and isoindol-1-one derivatives with high binding affinity to β-amyloid fibrils, Bioorg. Med. Chem. Lett., 18(5), pp. 1628-1631. DOI: 10.1016/j.bmcl.2008.01.066 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0960894X08000838 (accessed on 04.01.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Lee, H.J., Lim, S.J., Oh, S.J., Moon, D.H., Kim, D.J., Tae, J. &amp; Yoo, K.H. (2008) Isoindol-1,3-dione and isoindol-1-one derivatives with high binding affinity to β-amyloid fibrils, Bioorg. Med. Chem. Lett., 18(5), pp. 1628-1631. DOI: 10.1016/j.bmcl.2008.01.066 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0960894X08000838 (accessed on 04.01.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B11">
    <label>11.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Chirkov, Z.V., Kabanova, M.V., Filimonov, S.I., Abramov, I.G., Petzer, A., Petzer, J.P., Firgang, S.I. &amp; Suponitsky, K.Y. (2015) Inhibition of monoamine oxidase by indole-5, 6-dicarbonitrile derivatives, Bioorg. Med. Chem. Lett., 25(6), pp. 1206-1211. DOI: 10.1016/j.bmcl.2015.01.061 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0960894X15000827 (accessed on 03.05.2021).</mixed-citation>
     <mixed-citation xml:lang="en">Chirkov, Z.V., Kabanova, M.V., Filimonov, S.I., Abramov, I.G., Petzer, A., Petzer, J.P., Firgang, S.I. &amp; Suponitsky, K.Y. (2015) Inhibition of monoamine oxidase by indole-5, 6-dicarbonitrile derivatives, Bioorg. Med. Chem. Lett., 25(6), pp. 1206-1211. DOI: 10.1016/j.bmcl.2015.01.061 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0960894X15000827 (accessed on 03.05.2021).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B12">
    <label>12.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Meng, X.B., Han, D., Zhang, S.N., Guo, W., Cui, J.R. &amp; Li, Z.J. (2007) Synthesis and anti-inflammatory activity of N-phthalimidomethyl 2, 3-dideoxy-and 2, 3-unsaturated glycosides, Carbohydr. Res., 342(9), pp. 1169-1174. DOI: 10.1016/j.carres.2007.03.009 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0008621507001334 (accessed on 03.12.2021).</mixed-citation>
     <mixed-citation xml:lang="en">Meng, X.B., Han, D., Zhang, S.N., Guo, W., Cui, J.R. &amp; Li, Z.J. (2007) Synthesis and anti-inflammatory activity of N-phthalimidomethyl 2, 3-dideoxy-and 2, 3-unsaturated glycosides, Carbohydr. Res., 342(9), pp. 1169-1174. DOI: 10.1016/j.carres.2007.03.009 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0008621507001334 (accessed on 03.12.2021).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B13">
    <label>13.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Kabanova, M.V., Makarova, E.S., Chirkova, Z.V., &amp; Filimonov, S.I. (2021) Simplified method for obtaining 3-bromindol-5,6-dicarbonitrils from 1-hydroxindol-5,6-dicarbonitriles, From Chemistry Towards Technology Step-By-Step, 2(1), pp. 111-115. DOI: 10.52957/27821900_2021_01_111 [online]. Available at: http://chemintech.ru/index.php/tor/2021tom2no1 (accessed on 08.02.2021).</mixed-citation>
     <mixed-citation xml:lang="en">Kabanova, M.V., Makarova, E.S., Chirkova, Z.V., &amp; Filimonov, S.I. (2021) Simplified method for obtaining 3-bromindol-5,6-dicarbonitrils from 1-hydroxindol-5,6-dicarbonitriles, From Chemistry Towards Technology Step-By-Step, 2(1), pp. 111-115. DOI: 10.52957/27821900_2021_01_111 [online]. Available at: http://chemintech.ru/index.php/tor/2021tom2no1 (accessed on 08.02.2021).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B14">
    <label>14.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Abramov, I.G. &amp; Karpov, R.Z. (2020) Synthesis of 4-heterylamino-5-nitrophthalonitriles based on 4-bromo-5-nitrophthalonitrile, From Chemistry Towards Technology Step-By-Step, 1(1), pp. 62-67. DOI: 10.52957/27821900_2020_01_62 [online]. Available at: http://chemintech.ru/index.php/tor/ 2020tom1n1 (accessed on 03.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Abramov, I.G. &amp; Karpov, R.Z. (2020) Synthesis of 4-heterylamino-5-nitrophthalonitriles based on 4-bromo-5-nitrophthalonitrile, From Chemistry Towards Technology Step-By-Step, 1(1), pp. 62-67. DOI: 10.52957/27821900_2020_01_62 [online]. Available at: http://chemintech.ru/index.php/tor/ 2020tom1n1 (accessed on 03.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B15">
    <label>15.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Kotov, A.D., Kunichkina, A.S. &amp; Proskurina, I.K. (2021) Transformation of 5-halogen-3-aril-2,1-benzisoxazoles into quinazolines, From Chemistry Towards Technology Step-By-Step, 2(4), pp. 81-84. DOI: 10.52957/27821900_2021_04_81 [online]. Available at: http://chemintech.ru/index.php/tor/2021-2-4 (accessed on 11.011.2021).</mixed-citation>
     <mixed-citation xml:lang="en">Kotov, A.D., Kunichkina, A.S. &amp; Proskurina, I.K. (2021) Transformation of 5-halogen-3-aril-2,1-benzisoxazoles into quinazolines, From Chemistry Towards Technology Step-By-Step, 2(4), pp. 81-84. DOI: 10.52957/27821900_2021_04_81 [online]. Available at: http://chemintech.ru/index.php/tor/2021-2-4 (accessed on 11.011.2021).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B16">
    <label>16.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Filimonov, S.I., Makarova, E.S., Chirkova, Z.V. &amp; Kabanova, M.V. (2022) Diastereomeric composition of the reaction of the formation of hexahydro-5H-CHOMENO[4,3-D]PYRIDIN-5-ONES, From Chemistry Towards Technology Step-By-Step, 3(1), pp. 131-138. DOI: 10.52957/27821900_2022_01_131 [online]. Available at: http://chemintech.ru/index.php/tor/2022tom3no1 (accessed on 03.03.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Filimonov, S.I., Makarova, E.S., Chirkova, Z.V. &amp; Kabanova, M.V. (2022) Diastereomeric composition of the reaction of the formation of hexahydro-5H-CHOMENO[4,3-D]PYRIDIN-5-ONES, From Chemistry Towards Technology Step-By-Step, 3(1), pp. 131-138. DOI: 10.52957/27821900_2022_01_131 [online]. Available at: http://chemintech.ru/index.php/tor/2022tom3no1 (accessed on 03.03.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B17">
    <label>17.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Slastikhina, P.V., Chirkova, Z.V., Kabanova, M.V., Abramov, I.G., Filimonov, S.I., Begunov, R.S. &amp; Suponitsky, K.Y. (2020) Synthesis of substituted isoindole-1,3-diones with an amide fragment using the Schmidt rearrangement, Rus. Chem. Bull., 69, pp. 2378-2382. DOI: 10.1007/s11172-020-3027-9 [online]. Available at: https://link.springer.com/article/10.1007/s11172-020-3027-9#citeas (accessed on 23.05.2021).</mixed-citation>
     <mixed-citation xml:lang="en">Slastikhina, P.V., Chirkova, Z.V., Kabanova, M.V., Abramov, I.G., Filimonov, S.I., Begunov, R.S. &amp; Suponitsky, K.Y. (2020) Synthesis of substituted isoindole-1,3-diones with an amide fragment using the Schmidt rearrangement, Rus. Chem. Bull., 69, pp. 2378-2382. DOI: 10.1007/s11172-020-3027-9 [online]. Available at: https://link.springer.com/article/10.1007/s11172-020-3027-9#citeas (accessed on 23.05.2021).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B18">
    <label>18.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Desai, P., Schildknegt, K., Agrios, K.A., Mossman, C., Milligan, G.L. &amp; Aube, J. (2000) Reactions of alkyl azides and ketones as mediated by Lewis acids: Schmidt and Mannich reactions using azide precursors, J. Am. Chem. Soc., 122(30), pp. 7226-7232. DOI: 10.1021/ja000490v [online]. Available at: https://pubs.acs.org/doi/abs/10.1021/ja000490v (accessed on 03.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Desai, P., Schildknegt, K., Agrios, K.A., Mossman, C., Milligan, G.L. &amp; Aube, J. (2000) Reactions of alkyl azides and ketones as mediated by Lewis acids: Schmidt and Mannich reactions using azide precursors, J. Am. Chem. Soc., 122(30), pp. 7226-7232. DOI: 10.1021/ja000490v [online]. Available at: https://pubs.acs.org/doi/abs/10.1021/ja000490v (accessed on 03.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B19">
    <label>19.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Rokade, B.V., Prabhu, K.R. (2012) Chemoselective Schmidt reaction mediated by triflic acid: selective synthesis of nitriles from aldehydes, J. Org. Chem., 77(12), pp. 5364-5370. DOI: 10.1021/jo3008258 [online]. Available at: https://pubs.acs.org/doi/abs/10.1021/jo3008258 (accessed on 13.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Rokade, B.V., Prabhu, K.R. (2012) Chemoselective Schmidt reaction mediated by triflic acid: selective synthesis of nitriles from aldehydes, J. Org. Chem., 77(12), pp. 5364-5370. DOI: 10.1021/jo3008258 [online]. Available at: https://pubs.acs.org/doi/abs/10.1021/jo3008258 (accessed on 13.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B20">
    <label>20.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Filimonov, S.I., Chirkova, Z.V., Abramov, I.G., Firgang, S.I., Stashina, G.A., Strelenko, Y.A. &amp; Suponitsky, K.Y. (2012) Base-induced transformations of ortho-nitrobenzylketones: intramolecular displacement of nitro group versus nitro-nitrite rearrangement, Tetrahedron, 68(30), pp. 5991-5997. DOI: 10.1016/j.tet.2012.05.034 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0040402012007260 (accessed on 01.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Filimonov, S.I., Chirkova, Z.V., Abramov, I.G., Firgang, S.I., Stashina, G.A., Strelenko, Y.A. &amp; Suponitsky, K.Y. (2012) Base-induced transformations of ortho-nitrobenzylketones: intramolecular displacement of nitro group versus nitro-nitrite rearrangement, Tetrahedron, 68(30), pp. 5991-5997. DOI: 10.1016/j.tet.2012.05.034 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0040402012007260 (accessed on 01.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B21">
    <label>21.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Chirkova, Z.V., Kabanova, M.V., Filimonov, S.I., Abramov, I.G., Petzer, A., Petzer, J.P. &amp; Suponitsky, K.Y. (2016) An evaluation of synthetic indole derivatives as inhibitors of monoamine oxidase, Bioorg. Med. Chem. Lett., 26(9), pp. 2214-2219. DOI: 10.1016/j.bmcl.2016.03.060 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0960894X16302803 (accessed on 10. 04.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Chirkova, Z.V., Kabanova, M.V., Filimonov, S.I., Abramov, I.G., Petzer, A., Petzer, J.P. &amp; Suponitsky, K.Y. (2016) An evaluation of synthetic indole derivatives as inhibitors of monoamine oxidase, Bioorg. Med. Chem. Lett., 26(9), pp. 2214-2219. DOI: 10.1016/j.bmcl.2016.03.060 [online]. Available at: https://www.sciencedirect.com/science/article/pii/S0960894X16302803 (accessed on 10. 04.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B22">
    <label>22.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Suthar, Sh.K., Aggarwal, V., Chauhan, M., Sharma, A., Bansal, S. &amp; Sharma, M. (2015) Molecular docking and biological evaluation of hydroxysubstituted (Z)-3-benzylideneindolin-2-one chalcones for the lead identification as tyrosinase inhibitors, Med. Chem. Res., 24, pp. 1331–1341. DOI: 10.1007/s00044-014-1225-4 [online]. Available at: https://link.springer.com/article/10.1007/s00044-014-1225-4 (accessed on 11.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Suthar, Sh.K., Aggarwal, V., Chauhan, M., Sharma, A., Bansal, S. &amp; Sharma, M. (2015) Molecular docking and biological evaluation of hydroxysubstituted (Z)-3-benzylideneindolin-2-one chalcones for the lead identification as tyrosinase inhibitors, Med. Chem. Res., 24, pp. 1331–1341. DOI: 10.1007/s00044-014-1225-4 [online]. Available at: https://link.springer.com/article/10.1007/s00044-014-1225-4 (accessed on 11.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B23">
    <label>23.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Maroju, S., Podila, N.K., Velupula, G., Chittimalla, S. &amp; Pasad, T.R. (2018) Synthesis and Characterization of New (Z)‐5‐((1 H‐1, 2, 4‐Triazol‐1‐yl)methyl)‐3‐arylideneindolin‐2‐ones, J. Heterocycl. Chem., 56(1), pp. 153-157. DOI: 10.1002/jhet.3389 [online]. Available at: https://onlinelibrary.wiley.com/doi/abs/10.1002/jhet.3389 (accessed on 03.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Maroju, S., Podila, N.K., Velupula, G., Chittimalla, S. &amp; Pasad, T.R. (2018) Synthesis and Characterization of New (Z)‐5‐((1 H‐1, 2, 4‐Triazol‐1‐yl)methyl)‐3‐arylideneindolin‐2‐ones, J. Heterocycl. Chem., 56(1), pp. 153-157. DOI: 10.1002/jhet.3389 [online]. Available at: https://onlinelibrary.wiley.com/doi/abs/10.1002/jhet.3389 (accessed on 03.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B24">
    <label>24.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Tizzard, G.J., Coles, S.J., Edwards, M., Onyeabo, R.O., Allen, M. &amp; Spencer, J. (2013) Synthesis and solid-state characterisation of 4-substituted methylidene oxindoles, Chem. Central J., 7(1), pp. 1-10. DOI: 10.1186/1752-153X-7-182 [online]. Available at: https://bmcchem.biomedcentral.com/articles/10.1186/1752-153X-7-182 (accessed on 15.05.2022).</mixed-citation>
     <mixed-citation xml:lang="en">Tizzard, G.J., Coles, S.J., Edwards, M., Onyeabo, R.O., Allen, M. &amp; Spencer, J. (2013) Synthesis and solid-state characterisation of 4-substituted methylidene oxindoles, Chem. Central J., 7(1), pp. 1-10. DOI: 10.1186/1752-153X-7-182 [online]. Available at: https://bmcchem.biomedcentral.com/articles/10.1186/1752-153X-7-182 (accessed on 15.05.2022).</mixed-citation>
    </citation-alternatives>
   </ref>
  </ref-list>
 </back>
</article>
