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    	<title>IJPRS/V3/I3/00325 - 08/07/2014</title>

	<item>
		<title>Diversity Oriented Synthesis and Bio-evaluation of [1,2,4]triazolo[1,5-a]pyrimidine</title>
		
		<description><![CDATA[<h5>Author's Affiliation</h5>
		                                                <p></p>
		                                                <hr/>
                                                    	<h5>Abstract</h5>
		                                                <p>A simple, efficient, and diversity oriented synthesis and structural characterization of [1,2,4]triazolo[1,5-<em>a</em>]pyrimidine derivatives was undertaken using 5-amino,1,2,4-triazole as a building block. The synthesized compounds were fully characterized by spectroscopic techniques like FT-IR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, and mass spectroscopy. The biological evaluations of all synthesized compounds were also carried out.</p>
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                                                        <h5>Keywords</h5>
                                                         <p>[1,2,4] triazolo [1,5-<em>a</em>] pyrimidine, 5-amino,1,2,4-triazole, Diversity Oriented Synthesis, Spectroscopic Techniques</p>
                                                         
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                                                         <h5>Cite This Article</h5>
                                                         <p>Katariya, L. K., &amp; Kharadi, G. J. (2014). Diversity Oriented Synthesis and Bio-evaluation of [1,2,4]triazolo[1,5-a]pyrimidine. <em>International Journal for Pharmaceutical Research Scholars (IJPRS), 3(3),</em> 14-25.</p>                                                         <hr/>
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		<link>https://www.ijprs.com/article/diversity-oriented-synthesis-and-bio-evaluation-of-124triazolo15-apyrimidine/</link>
		<author>Katariya, L. K., Kharadi, G. J.        </author>

		<pdflink>http://www.ijprs.com/wp-content/uploads/2018/09/IJPRS-V3-I3-000325.pdf</pdflink>

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