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  <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">AJPTR66009</article-id>
      <title-group>
        <article-title>One Spot Synthesis of New N-Substituted Acridinediones by Hantzsch condensation</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Wani</surname>
            <given-names>Nazir Ahmad</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date pub-type="epub" iso-8601-date="2016-12-01">
        <month>12</month>
        <day>01</day>
        <year>2016</year>
      </pub-date>
      <volume>6</volume>
      <issue>6</issue>
      <abstract>
        <p>Acridinediones were synthesized by the one-pot Hantzsch condensation of an aromatic amines, 2-(4-floro phenyl)-5-bis(1,3diketo-5,5-dimethyl cyclohexyl)methylfuran  in acetic acid and the reaction mixture is refluxed for eighteen hours, the crushed ice the solid obtained was filtered and purified by column chromatography. The compound was characterized by using different spectrochemical characterizations.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Acridinediones</kwd>
        <kwd>Hantzsch condensation</kwd>
        <kwd>Aromatic amine</kwd>
        <kwd>Column Chromatography.</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
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