<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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-184</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>Статьи</subject></subj-group></article-categories><title-group><article-title>Синтез производных м-терфенила в качестве стабилизаторов полимерных материалов</article-title><trans-title-group xml:lang="en"><trans-title>Synthesis of m-terphenyl derivatives as polymer stabilizers</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>Бойко</surname><given-names>Д. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Boiko</surname><given-names>D. P.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Курлович</surname><given-names>А. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Kurlovich</surname><given-names>A. L.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Тарасевич</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Tarasevich</surname><given-names>V. A.</given-names></name></name-alternatives><email xlink:type="simple">tar@ichnm.basnet.by</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт химии новых материалов НАН Беларуси</institution></aff><aff xml:lang="en"><institution>Institute of Chemistry of New Materials of the National Academy of Sciences of Belarus</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>08</day><month>06</month><year>2016</year></pub-date><volume>0</volume><issue>1</issue><fpage>122</fpage><lpage>128</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Бойко Д.П., Курлович А.Л., Тарасевич В.А., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Бойко Д.П., Курлович А.Л., Тарасевич В.А.</copyright-holder><copyright-holder xml:lang="en">Boiko D.P., Kurlovich A.L., Tarasevich V.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/184">https://vestichem.belnauka.by/jour/article/view/184</self-uri><abstract><p>Рассмотрены методы синтеза производных м-терфенила - эффективных стабилизаторов полимерных материалов, антиокислителей пищевых продуктов, консервантов медицинских препаратов.</p></abstract><trans-abstract xml:lang="en"><p>Methods for synthesis of m-terphenyl derivatives used as effective polymeric material stabilizers, food antioxidants, medicine preservatives have been discussed.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>2'-гидрокси-м-терфенил</kwd><kwd>реактив Гриньяра</kwd><kwd>реакции кросс-сочетания</kwd><kwd>халкон</kwd><kwd>2'-hydroxy-m-terphenyl</kwd><kwd>Grignard reagents</kwd><kwd>cross-coupling reactions</kwd><kwd>chalcone</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">Фенольные антиоксиданты - высокоэффективные стабилизаторы полимеров и материалов различного назначения / А. В. Кучин [и др.] // Изв. УНЦ РАН. Химия. - 2012. - № 4. - С. 80-93.</mixed-citation><mixed-citation xml:lang="en">Фенольные антиоксиданты - высокоэффективные стабилизаторы полимеров и материалов различного назначения / А. В. Кучин [и др.] // Изв. УНЦ РАН. Химия. - 2012. - № 4. - С. 80-93.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Synthesis of new polymeric stabilizers for polymers / J. Q. Pan [et al.] // J. Appl. Polym. Sci. - 2000. - Vol. 78, № 2. - Р. 403-411.</mixed-citation><mixed-citation xml:lang="en">Synthesis of new polymeric stabilizers for polymers / J. Q. Pan [et al.] // J. Appl. Polym. Sci. - 2000. - Vol. 78, № 2. - Р. 403-411.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Gachter, R. Plastics additives handbook: stabilizers, processing AIDS, plasticizers, fillers, reinforcements, colorants for thermoplastics / R. Gachter, H. Muller. - 4th. Edition, revised and enlarged. - Cincinnati: Hanser-Gardner Publications Inc., 1993. - P. 1025.</mixed-citation><mixed-citation xml:lang="en">Gachter, R. Plastics additives handbook: stabilizers, processing AIDS, plasticizers, fillers, reinforcements, colorants for thermoplastics / R. Gachter, H. Muller. - 4th. Edition, revised and enlarged. - Cincinnati: Hanser-Gardner Publications Inc., 1993. - P. 1025.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Liu, J.-K. Natural terphenyls: developments since 1877 / J.-K. Liu // Chemical Reviews. - 2006. - Vol. 106. - P. 2209-2223.</mixed-citation><mixed-citation xml:lang="en">Liu, J.-K. Natural terphenyls: developments since 1877 / J.-K. Liu // Chemical Reviews. - 2006. - Vol. 106. - P. 2209-2223.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Substituent effects on the bond dissociation enthalpies of aromatic amines / D. Pratt [et al.] // J. of the American Chemical Society. - 2002. - Vol. 124, № 37. - P. 11085-11092.</mixed-citation><mixed-citation xml:lang="en">Substituent effects on the bond dissociation enthalpies of aromatic amines / D. Pratt [et al.] // J. of the American Chemical Society. - 2002. - Vol. 124, № 37. - P. 11085-11092.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">De Jonge, C. R. H. I. Synergism of antioxidants / C. R. H. I. de Jonge // Pure and Applied Chemistry. - 1983. - Vol. 55, № 10. - P. 1637-1650.</mixed-citation><mixed-citation xml:lang="en">De Jonge, C. R. H. I. Synergism of antioxidants / C. R. H. I. de Jonge // Pure and Applied Chemistry. - 1983. - Vol. 55, № 10. - P. 1637-1650.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Hay, A. S. Poly(phenylene oxide)s and poly(arylene ether)s derived from 2,6-diarylphenols / A. S. Hay // Progress in Polymer Science. - 1999. - Vol. 24, N 1. - P. 45-80.</mixed-citation><mixed-citation xml:lang="en">Hay, A. S. Poly(phenylene oxide)s and poly(arylene ether)s derived from 2,6-diarylphenols / A. S. Hay // Progress in Polymer Science. - 1999. - Vol. 24, N 1. - P. 45-80.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Yang, H. Synthesis of symmetrically substituted 2,6-diphenylphenols / H. Yang, A. S. Hay // Synthesis. - 1992. -Vol. 5. - P. 467-472.</mixed-citation><mixed-citation xml:lang="en">Yang, H. Synthesis of symmetrically substituted 2,6-diphenylphenols / H. Yang, A. S. Hay // Synthesis. - 1992. -Vol. 5. - P. 467-472.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Awasung, K. // Undergrad. Rev. 2008. Vol. 4. P. 71-78.</mixed-citation><mixed-citation xml:lang="en">Awasung, K. // Undergrad. Rev. 2008. Vol. 4. P. 71-78.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Suzuki, A. Cross-coupling reactions via organoboranes / A. Suzuki // J. of Organometallic Chemistry. - 2002. -Vol. 653, N 1. - P. 83-90.</mixed-citation><mixed-citation xml:lang="en">Suzuki, A. Cross-coupling reactions via organoboranes / A. Suzuki // J. of Organometallic Chemistry. - 2002. -Vol. 653, N 1. - P. 83-90.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Suzuki-Miyaura cross-coupling in acylation reactions, scope and recent developments / M. Blangetti [et al.] // Molecules. - 2013. - Vol. 18, N 1. - P. 1188-1213.</mixed-citation><mixed-citation xml:lang="en">Suzuki-Miyaura cross-coupling in acylation reactions, scope and recent developments / M. Blangetti [et al.] // Molecules. - 2013. - Vol. 18, N 1. - P. 1188-1213.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Reference scales for the characterization of cationic electrophiles and neutral nucleophiles / H. Mayr [et al.] // J. of the American Chemical Society. - 2001. - Vol. 123, N 39. - P. 9500-9512.</mixed-citation><mixed-citation xml:lang="en">Reference scales for the characterization of cationic electrophiles and neutral nucleophiles / H. Mayr [et al.] // J. of the American Chemical Society. - 2001. - Vol. 123, N 39. - P. 9500-9512.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Lucius, R. Kinetische untersuchungen von carbokation-carbanion-kombinationen: schlussel zu einem allgemeinen modell polarer organischer reaktivitat / R. Lucius, R. Loos, H. Mayr // Angewandte Chemie International Edition. - 2002. -Vol. 41. - P. 91-95.</mixed-citation><mixed-citation xml:lang="en">Lucius, R. Kinetische untersuchungen von carbokation-carbanion-kombinationen: schlussel zu einem allgemeinen modell polarer organischer reaktivitat / R. Lucius, R. Loos, H. Mayr // Angewandte Chemie International Edition. - 2002. -Vol. 41. - P. 91-95.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Loos, R. Ambident reactivity of the thiocyanate anion revisited: Can the product ratio be explained by the hard soft acid base principle / R. Loos, S. Kobayashi, H. Mayr // J. of the American Сhemical Society. - 2003. - Vol. 125, N 46. -P. 14126-14132.</mixed-citation><mixed-citation xml:lang="en">Loos, R. Ambident reactivity of the thiocyanate anion revisited: Can the product ratio be explained by the hard soft acid base principle / R. Loos, S. Kobayashi, H. Mayr // J. of the American Сhemical Society. - 2003. - Vol. 125, N 46. -P. 14126-14132.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Specific inhibitory of tyrosine-specific protein kinase. I. Synthesis and inhibitory activities of α-cyanocinnamamides / T. Shiraishi [et al.] // Chemical and Pharmaceutical Bulletin - 1988. - Vol. 36, N 3. - P. 974-981.</mixed-citation><mixed-citation xml:lang="en">Specific inhibitory of tyrosine-specific protein kinase. I. Synthesis and inhibitory activities of α-cyanocinnamamides / T. Shiraishi [et al.] // Chemical and Pharmaceutical Bulletin - 1988. - Vol. 36, N 3. - P. 974-981.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Курлович, А. Л. Синтез новых имино- и аминопроизводных на основе 2'-гидрокси[1,1';3',1"]терфенил-5'-карбальдегида / А. Л. Курлович, В. А. Тарасевич, Н. Г. Козлов // Весці Нац. акад. навук Беларусі. Сер. хiм. навук. -2011. - N 1. - С. 45-48.</mixed-citation><mixed-citation xml:lang="en">Курлович, А. Л. Синтез новых имино- и аминопроизводных на основе 2'-гидрокси[1,1';3',1"]терфенил-5'-карбальдегида / А. Л. Курлович, В. А. Тарасевич, Н. Г. Козлов // Весці Нац. акад. навук Беларусі. Сер. хiм. навук. -2011. - N 1. - С. 45-48.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Курлович, А. Л. Реакция 2'-гидрокси[1, 1'; 3', Г']терфенил-5-карбальдегида с 1-нафтиламином, 8-хинолинамином и 1, 3-дикетонами / А. Л. Курлович, В. А. Тарасевич, Н. Г. Козлов // Журн. орган. химии. - 2009. - Т. 45, № 10. -С. 1519-1524.</mixed-citation><mixed-citation xml:lang="en">Курлович, А. Л. Реакция 2'-гидрокси[1, 1'; 3', Г']терфенил-5-карбальдегида с 1-нафтиламином, 8-хинолинамином и 1, 3-дикетонами / А. Л. Курлович, В. А. Тарасевич, Н. Г. Козлов // Журн. орган. химии. - 2009. - Т. 45, № 10. -С. 1519-1524.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Курлович, А. Л. Продукты реакции 2'-гидрокси[1,1';3',1'']терфенил-5'-карбальдегида с n-толуидином и 1,3-дикетонами / А. Л. Курлович, В. А. Тарасевич, Н. Г. Козлов // Весці Нац. акад. навук Беларусі. Сер. хiм. навук. - 2010. -№ 4. - С. 79-84.</mixed-citation><mixed-citation xml:lang="en">Курлович, А. Л. Продукты реакции 2'-гидрокси[1,1';3',1'']терфенил-5'-карбальдегида с n-толуидином и 1,3-дикетонами / А. Л. Курлович, В. А. Тарасевич, Н. Г. Козлов // Весці Нац. акад. навук Беларусі. Сер. хiм. навук. - 2010. -№ 4. - С. 79-84.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Курлович, А. Л. Синтез спироциклических производных азафенантрена, содержащих гидрокси-м-терфенильный фрагмент / А. Л. Курлович, В. А. Тарасевич, Н. Г. Козлов // Журн. орган. химии. - 2010. - Т. 46, № 9. - С. 1324-1327.</mixed-citation><mixed-citation xml:lang="en">Курлович, А. Л. Синтез спироциклических производных азафенантрена, содержащих гидрокси-м-терфенильный фрагмент / А. Л. Курлович, В. А. Тарасевич, Н. Г. Козлов // Журн. орган. химии. - 2010. - Т. 46, № 9. - С. 1324-1327.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Synthesis, characterization and biological evaluation of some new functionalized terphenyl derivatives / S. Samshuddin [et. al] // International Journal of Medicinal Chemistry. - 2012. - P. 1-13.</mixed-citation><mixed-citation xml:lang="en">Synthesis, characterization and biological evaluation of some new functionalized terphenyl derivatives / S. Samshuddin [et. al] // International Journal of Medicinal Chemistry. - 2012. - P. 1-13.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
