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    	<title>IJPRS/V2/I4/00211 - 27/11/2013</title>

	<item>
		<title>Synthetic Advances and Biological Activities of 4-Hydroxy Coumarin Derivatives</title>
		
		<description><![CDATA[<h5>Author's Affiliation</h5>
		                                                <p></p>
		                                                <hr/>
                                                    	<h5>Abstract</h5>
		                                                <p>Synthesis of a series of 4-hydroxy-6-methyl-3-(substituted methyl)-2H-chromen-2-one. (4a-g) was achieved from different secondary amine, formaldehyde and 4-hydroxy-6-methyl-2H-chromen-2-one using Con HCl added and refluxed within 8 hrs with good yield. The structures of the products were supported by FTIR, PMR and mass spectral data.</p>
                                                    	<hr/>
                                                        <h5>Keywords</h5>
                                                         <p>4-hydroxy-6-methyl-3-(substituted methyl)-2H-chromen-2-one; secondary amine, 2-Aformaldehyde, only refluxed</p>
                                                         
                                                    	                                                    	<hr/>
                                                         <h5>Cite This Article</h5>
                                                         <p>Karia, D. C., Pancholi, K. S., &amp; Varu, R. A. (2013). Synthetic Advances and Biological Activities of 4-Hydroxy Coumarin Derivatives. <em>International Journal for Pharmaceutical Research Scholars (IJPRS), 2(4),</em> 139-142.</p>                                                         <hr/>
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		<link>https://www.ijprs.com/article/synthetic-advances-and-biological-activities-of-4-hydroxy-coumarin-derivatives/</link>
		<author>Karia, D. C., Pancholi, K. S., Varu, R. A.        </author>

		<pdflink>http://www.ijprs.com/wp-content/uploads/2018/09/IJPRS-V2-I4-00211.pdf</pdflink>

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