<?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>December 2007</publicationDate>
    <volume>3</volume>
    <issue>1</issue>
    <startPage>69</startPage>
    <endPage>72</endPage>
    <doi>juc</doi>
    <publisherRecordId>791</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis of 2-(1- substitutedguanidino-3-yl)-4- (3-phenylthiocarbamido- 1-yl)-6-substitutedimino-1,3,5-thiadiazine </title>
    <authors>
      <author>
        <name>M.E. Shelke (mesheike@rediffmail.com)</name>
        <affiliationId>1</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">Department of Chemistry, H.V.P.M. College, of Engg. and Tech. HVPM, Campus, Amravati, (M.S.) INDIA</affiliationName>
    </affiliationsList>
    <abstract language="eng">&lt;p&gt;Novel series 2-(1-substitutedguanidino-3-yl)-4-(3-phenylthiocarbamido -1-yl)-6- substitutedimino-1,3,5-thiadiazine [3a(i) to 3f(ii)] have been obtained by basification of their hydrochlorides [2a(i) to 2f(ii)] in presence of ammonium hydroxide solution, which are synthesized by the interaction of 1-Formamidino- (N-phenylthioamido)-5-phenyl-2-thio-4-iminobiuret (1a-f) and N-aryl/alkylisocyanodichlorides. The latter were prepared initially by the condensation of substitutedisothiocyanate with N phenylformamidinoformamidinothiocarbamide. The structure of all these compounds were established on the basis of elemental analysis, IR and PMR spectral data.&lt;/p&gt;&#xD;
</abstract>
    <fullTextUrl format="html">https://journalofchemistry.org/paper/791/</fullTextUrl>
    <keywords>
      <keyword language="eng">substitutedguanidino</keyword>
    </keywords>
    <keywords>
      <keyword language="eng">thiadiazine</keyword>
    </keywords>
  </record>
</records>
