<?xml version="1.0"?>
<records>
  <record>
    <language>eng</language>
    <publisher>Ansari Education and Research Society</publisher>
    <journalTitle>Journal of Ultra Chemistry</journalTitle>
    <issn>0973-3450</issn>
    <eissn>2319-8036</eissn>
    <publicationDate>June 2006</publicationDate>
    <volume>2</volume>
    <issue>2</issue>
    <startPage>41</startPage>
    <endPage>44</endPage>
    <doi>juc</doi>
    <publisherRecordId>803</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis of some antimicrobial 3-Aryl-1,2,4- triazolo-8-methyl-thiadiazepin-6-ones </title>
    <authors>
      <author>
        <name>H.K. Singh (hemnt38singh@yahoo.com</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name> S. Singh</name>
        <affiliationId>1</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">Department of Chemistry, T.D.P.G., College, Jaunpur, (V.B.S.) Purvachal Universtiy, Jaunpur (U.P.) 222002 (INDIA)</affiliationName>
    </affiliationsList>
    <abstract language="eng">&lt;p style="text-align: justify;"&gt;Cyclodehydration of thiocarbohydrazide with substituted benzoic acid gives, 5-Aryl-4-amino-3-mercapto-1,2,4 triazole.&amp;nbsp; The requisite 3-Aryl-1,2,4-triazolo-8-methyl-thiadiazepin-6-ones were prepared by refluxing ethyl acetoacetate and 5-Aryl-4-amino-3-mercapto-1,2,4-triazole. The screening results are correlated with the structural features of the tested compounds.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/p&gt;&#xD;
</abstract>
    <fullTextUrl format="html">https://journalofchemistry.org/paper/803/</fullTextUrl>
    <keywords>
      <keyword language="eng">Synthesis of some antimicrobial </keyword>
    </keywords>
    <keywords>
      <keyword language="eng">ones </keyword>
    </keywords>
  </record>
</records>
