<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Article Tag Suite 1.1//EN"
  "https://jats.nlm.nih.gov/publishing/1.1/JATS-journalpublishing1.dtd">
<article xmlns:xlink="http://www.w3.org/1999/xlink"
         xmlns:mml="http://www.w3.org/1998/Math/MathML"
         article-type="research-article"
         xml:lang="en">
  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>American Journal of PharmTech Research</journal-title>
        <abbrev-journal-title abbrev-type="publisher">AJPTR</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2249-3387</issn>
      <publisher>
        <publisher-name>undefined</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">AJPTR53049</article-id>
      <title-group>
        <article-title>Synthesis and Anti-Microbial Activity of the Highly Substituted 2-(1H-Benzo[d] Imidazol-2-yl)-3-Oxobutanenitrile</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Patil</surname>
            <given-names>S. K.</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Chandan</surname>
            <given-names>N S</given-names>
          </name>
          <xref ref-type="aff" rid="aff2"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Nirmalkar</surname>
            <given-names>A S</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
      </contrib-group>
      <aff id="aff1">Department of Chemistry, CKT College of ACS, New Panvel, M.S. India.</aff>
      <aff id="aff2">Department of Chemistry, Siddharth college of ASC, Fort Mumbai, M.S. India.</aff>
      <pub-date pub-type="epub" iso-8601-date="2015-06-01">
        <month>06</month>
        <day>01</day>
        <year>2015</year>
      </pub-date>
      <volume>5</volume>
      <issue>3</issue>
      <abstract>
        <p>Imidazoles are nitrogen containing heterocyclic compounds, widely present in nature. The imidazole ring is a part of several important natural products, including purine, histamine, histidine and nucleic acid. Highly substituted imidazoles derivatives belong to a crucial structural motif that is seen in many pharmaceutically and biologically interesting molecules. They have been intensively used in medicinal chemistry as drugs such as antihistaminic1, antiulcerative,2 antihelmentic,3 and antipsychotic.4 Several benzimidazoles have been reported as antiviral,7 anticoagulant,8 antiinflammatory,9 antibacterial10 and anticancer agents.11 The present work deals with the derivatization of 2-(1H-benzo[d]imidazol-2-yl)-3-oxobutanenitrile with thiazolidin-4-one, oxazolidin-4-one and azetidin-2-one and characterization. All the compounds were tested for biological activity against E. coli, S. typhi, S. aureus while streptomycin was used as standard.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Imidazoles</kwd>
        <kwd>Benzimidazole</kwd>
        <kwd>Heterocyclic compound.</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <!-- Full article body not available in metadata-only JATS export. See PDF/HTML galley. -->
  </body>
  <back/>
</article>
