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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">Anti-Infective Agents</journal-id><journal-title-group><journal-title xml:lang="en">Anti-Infective Agents</journal-title><trans-title-group xml:lang="ru"><trans-title>Anti-Infective Agents</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2211-3525</issn><issn publication-format="electronic">2211-3533</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">642305</article-id><article-id pub-id-type="doi">10.2174/0122113525276208231116121402</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Medicine</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">Recent Trends on Synthesis of Benzimidazoles</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>El-Rashedy</surname><given-names>Ahmed</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Magd El-Din</surname><given-names>Asmaa</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Yousif</surname><given-names>Nabil</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Yousif</surname><given-names>Mahmoud</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff id="aff1"><institution>Department of Natural and Microbial Products, National Research Center, Cairo, Egypt</institution></aff><aff id="aff2"><institution>Department of Photochemistry,
Chemical Industries Research Institute, National Research Centre, Cairo, Egypt</institution></aff><pub-date date-type="pub" iso-8601-date="2024-04-01" publication-format="electronic"><day>01</day><month>04</month><year>2024</year></pub-date><volume>22</volume><issue>2</issue><issue-title xml:lang="ru"/><history><date date-type="received" iso-8601-date="2024-11-27"><day>27</day><month>11</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://journals.eco-vector.com/2211-3525/article/view/642305">https://journals.eco-vector.com/2211-3525/article/view/642305</self-uri><abstract xml:lang="en"><p id="idm45507060744352">Preparation of benzimidazole derivatives have become the interest of many chemists because of the versatile therapeutic activity of benzimidazoles as antiulcer, antimicrobial, anti-viral, anticancer, anti-inflammatory, analgesic and anthelmintic drugs. This review will de-scribe the most recent research on benzimidazole synthesis.</p></abstract><kwd-group xml:lang="en"><kwd>Benzimidazole</kwd><kwd>2,5-dimethyl benzimidazole</kwd><kwd>2-subsitituted benzimidazole</kwd><kwd>o-Phenylene diamine</kwd><kwd>5-methyl benzimidazole</kwd><kwd>6-dimethylbenzimidazole.</kwd></kwd-group></article-meta></front><body></body><back><ref-list/></back></article>
