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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">AJPTR43052</article-id>
      <title-group>
        <article-title>Microwave Initiated Synthesis of Pyrimidine Analogues and Study of their Antimicrobial Properties</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Lal</surname>
            <given-names>Kundan</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>J.Paliwal</surname>
            <given-names>L.</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>M.B.Bagade</surname>
            <given-names>M.B.Bagade</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date pub-type="epub" iso-8601-date="2014-06-01">
        <month>06</month>
        <day>01</day>
        <year>2014</year>
      </pub-date>
      <volume>4</volume>
      <issue>3</issue>
      <abstract>
        <p>An efficient and convenient multi component reaction for the synthesis of 2-Imino-4,6-diaryldihydropyrimidines scaffolds have been accomplished from chalcones and guanidine hydrochloride in the presence of a catalytic amount of an alkali under solvent-free conditions using microwave irradiation.  The synthesized pyrimidines have been characterized on the basis of their chemical properties and spectroscopic data.  Operational simplicity, short reaction times, excellent yields and environmentally-benign conditions are the other advantages of this protocol. Using this method, we have synthesized some new pyrimidines with antimicrobial properties and high chemical yields in much short reaction times.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Solvent- free</kwd>
        <kwd>Antibacterial</kwd>
        <kwd>Chalcones</kwd>
        <kwd>Biological activity</kwd>
        <kwd>Green Chemistry</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
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