<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet type="text/xsl" href="https://www.eurjchem.com/lib/pkp/xml/oai2.xsl" ?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/"
	xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"
	xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/
		http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
	<responseDate>2026-04-05T15:36:41Z</responseDate>
	<request identifier="oai:ojs.www.eurjchem.com:article/788" metadataPrefix="oai_dc" verb="GetRecord">https://www.eurjchem.com/index.php/eurjchem/oai</request>
	<GetRecord>
		<record>
			<header>
				<identifier>oai:ojs.www.eurjchem.com:article/788</identifier>
				<datestamp>2013-09-30T04:22:07Z</datestamp>
				<setSpec>eurjchem:ART</setSpec>
				<setSpec>driver</setSpec>
			</header>
			<metadata>
<oai_dc:dc
	xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"
	xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/
	http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en-US">Activated bentonite promoted Friedländer condensation reactions: Synthesis of thieno[2,3-b]quinolinones and tacrines analogues derivatives</dc:title>
	<dc:creator>Dridi, Khaireddine Mohamed</dc:creator>
	<dc:creator>Said, Ridha Ben</dc:creator>
	<dc:creator>Arfaoui, Youssef</dc:creator>
	<dc:creator>Al-Ayed, Abdullah Sulaiman</dc:creator>
	<dc:subject xml:lang="en-US">Ketones</dc:subject>
	<dc:subject xml:lang="en-US">Bentonite</dc:subject>
	<dc:subject xml:lang="en-US">Tacrine analogues</dc:subject>
	<dc:subject xml:lang="en-US">Friedlander reaction</dc:subject>
	<dc:subject xml:lang="en-US">2-Aminothiophene-3-carbonitrile</dc:subject>
	<dc:subject xml:lang="en-US">4-Aminothieno[2</dc:subject>
	<dc:subject xml:lang="en-US">3-b]quinolinones</dc:subject>
	<dc:description xml:lang="en-US">Some new aminothieno[2,3-b]quinolinones and tacrine analogues derivatives were synthesized in high yield with acid activated bentonite as a catalyst via the Friedländer condensation reactions between 2-aminothiophene-3-carbonitrile and ketones. The structure elucidation of compounds was done by FT-IR, NMR spectroscopy and microanalytical elemental data.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2013-09-30</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/788</dc:identifier>
	<dc:identifier>10.5155/eurjchem.4.3.216-219.788</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 4 No. 3 (2013): September 2013; 216-219</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/788/PDF</dc:relation>
</oai_dc:dc>
			</metadata>
		</record>
	</GetRecord>
</OAI-PMH>
