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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Priroda</journal-id><journal-title-group><journal-title xml:lang="en">Priroda</journal-title><trans-title-group xml:lang="ru"><trans-title>Природа</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0032-874X</issn><publisher><publisher-name xml:lang="en">Akademizdatcenter Nauka</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">628088</article-id><article-id pub-id-type="doi">10.7868/S0032874X21120061</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">2021 Nobel Prize Laureates in Chemistry: Benjamin List and David W.C.MacMillan</article-title><trans-title-group xml:lang="ru"><trans-title>Лауреаты Нобелевской премии 2021 года. По химии — Беньямин Лист и Дэвид МакМиллан</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zlotin</surname><given-names>S. G</given-names></name><name xml:lang="ru"><surname>Злотин</surname><given-names>С. Г</given-names></name></name-alternatives><email>zlotin@ioc.ac.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Zelinsky Institute of Organic Chemistry, RAS</institution></aff><aff><institution xml:lang="ru">Институт органической химии имени Н.Д. Зелинского РАН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2021-12-16" publication-format="electronic"><day>16</day><month>12</month><year>2021</year></pub-date><issue>12</issue><issue-title xml:lang="en">NO12 (2021)</issue-title><issue-title xml:lang="ru">№12 (2021)</issue-title><fpage>35</fpage><lpage>44</lpage><history><date date-type="received" iso-8601-date="2024-03-02"><day>02</day><month>03</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="ru">Copyright ©; 2021, Издательство «Наука»</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Издательство «Наука»</copyright-holder></permissions><self-uri xlink:href="https://journals.eco-vector.com/0032-874X/article/view/628088">https://journals.eco-vector.com/0032-874X/article/view/628088</self-uri><abstract xml:lang="en"><p>In 2021 the Nobel Prize of Chemistry was awarded to professors Benjamin List of the Max Planck Institute for Coal Research (Germany) and David W.C.MacMillan of the Princeton University (USA) “for the development of asymmetric organocatalysis”, a method that uses small organic molecules as catalysts instead of enzymes or metals. This innovation in molecular construction has led to catalysts that are convenient in handling, less expensive, and environmentally friendly. Asymmetric organocatalysis is especially important to the drug discovery process. Biologically active molecules are often chiral, and organocatalysts provide a way to make candidate drug compounds enantioselectively, efficiently and quickly.</p></abstract><trans-abstract xml:lang="ru"><p>В 2021 г. Нобелевская премия по химии присуждена профессорам Беньямину Листу из Института исследования угля Общества Макса Планка (Германия) и Дэвиду МакМиллану из Принстонского университета (США) за разработку асимметрического органокатализа — метода органического синтеза, основанного на применении в качестве катализаторов малых хиральных «безметальных» органических молекул (органокатализаторов). Преимуществом органокатализаторов перед металлокомплексными катализаторами и ферментами является их меньшая стоимость, простота в обращении и экологичность (зеленая химия). Метод открывает новые возможности для создания более эффективных и лишенных вредных побочных эффектов энантиомерно чистых лекарственных препаратов.</p></trans-abstract><kwd-group xml:lang="en"><kwd>Nobel Prize</kwd><kwd>asymmetric organocatalysis</kwd><kwd>enantioselective synthesis</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>Нобелевская премия</kwd><kwd>асимметрический органокатализ</kwd><kwd>энантиоселективный синтез</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Vineyard B.D., Knowles W.S., Sabacky M.J. et al. Asymmetric hydrogenation. Rhodium chiral bisphosphine catalyst. J. Am. Chem. Soc. 1977; 99(18): 5946–5952. DOI:10.1021/ja00460a018.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Noyori R., Hashiguchi S. 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