<?xml version="1.0" encoding="UTF-8"?><article>
	<front>
		<journal-meta>
			<journal-id journal-id-type="publisher">GJRA</journal-id>
			<journal-title>GJRA - Global Journal For Research Analysis</journal-title>
			<issn pub-type="ppub">2250 - 1991</issn>
			<publisher>
				<publisher-name>Indian Society for Health and Advanced Research</publisher-name>
			</publisher>
		</journal-meta>
		<article-meta>
			<article-id pub-id-type="other">gjra-5-12-5965</article-id>
			<article-categories>
				<subj-group>
					<subject>Original Research Paper</subject>
				</subj-group>
			</article-categories>
			<title-group>
				<article-title>ANALOGUES OF 6,8-DIBROMOQUINAZOLIN-4(3H) ONES: POTENTIAL ANTIMICROBIAL AGENTS IN VITRO</article-title>
			</title-group>
			<contrib-group><contrib contrib-type="author">
						<name>
							<surname>G.</surname>
							<given-names>Barat</given-names>
							<prefix>Dr.</prefix>
						</name>
						<xref ref-type="aff" rid="aff000">
							<sup></sup>
						</xref>
						</contrib></contrib-group><pub-date pub-type="ppub">
				<month>December</month>
				<year>2016</year>
			</pub-date>
			<volume>5</volume>
			<issue>12</issue>
			<fpage>01</fpage>
			<lpage>02</lpage>
			<abstract>
				<title>ABSTRACT</title>
				<p>&amp;lt;p&amp;gt;&amp;amp;nbsp;&amp;lt;span style=&quot;text-align: justify; vertical-align: baseline;&quot;&amp;gt;A new series of some analogues of 6,8-dibromoquinazolin-4(3&amp;lt;i&amp;gt;H&amp;lt;/i&amp;gt;)-ones &amp;lt;b&amp;gt;6&amp;lt;/b&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;b style=&quot;text-align: justify;&quot;&amp;gt;&amp;lt;sub&amp;gt;1-12&amp;lt;/sub&amp;gt;&amp;lt;/b&amp;gt;&amp;lt;span style=&quot;text-align: justify; vertical-align: baseline;&quot;&amp;gt; have been synthesized by the cyclisation of acrylamide &amp;lt;b&amp;gt;5&amp;lt;/b&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;b style=&quot;text-align: justify;&quot;&amp;gt;&amp;lt;sub&amp;gt;1-12&amp;lt;/sub&amp;gt;&amp;lt;/b&amp;gt;&amp;lt;b style=&quot;text-align: justify;&quot;&amp;gt;&amp;lt;span style=&quot;vertical-align:&amp;amp;#10;baseline&quot;&amp;gt; &amp;lt;/span&amp;gt;&amp;lt;/b&amp;gt;&amp;lt;span style=&quot;text-align: justify; vertical-align: baseline;&quot;&amp;gt;with&amp;lt;b&amp;gt; &amp;lt;/b&amp;gt;hydrazine hydrate. The overall reaction was based catalysed conventional multistep process. The title compounds have been characterized by spectral data IR, &amp;lt;/span&amp;gt;&amp;lt;span style=&quot;text-align: justify;&quot;&amp;gt;1&amp;lt;/span&amp;gt;&amp;lt;span style=&quot;text-align: justify; vertical-align: baseline;&quot;&amp;gt;H NMR, &amp;lt;/span&amp;gt;&amp;lt;span style=&quot;text-align: justify;&quot;&amp;gt;13&amp;lt;/span&amp;gt;&amp;lt;span style=&quot;text-align: justify; vertical-align: baseline;&quot;&amp;gt;C NMR and elemental analysis. All the synthesized compounds were screened for antibacterial and fungicidal activity &amp;lt;i&amp;gt;In Vitro&amp;lt;/i&amp;gt; by disc diffusion method and strength compare with standard drug. &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp;&amp;lt;/span&amp;gt;&amp;lt;/p&amp;gt;
&amp;lt;p class=&quot;MsoNormal&quot; style=&quot;text-align:justify;line-height:200%&quot;&amp;gt;&amp;lt;span style=&quot;vertical-align:&amp;amp;#10;baseline&quot;&amp;gt;&amp;amp;nbsp;&amp;lt;br /&amp;gt;
&amp;lt;o:p&amp;gt;&amp;lt;/o:p&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/p&amp;gt;</p>
			</abstract>			
			<counts>
				<ref-count count="7"/>
				<page-count count="2"/>
			</counts>
		</article-meta>
	</front>
</article>