<?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>2026-04-24T10:52:35Z</responseDate>
	<request identifier="oai:ojs.www.eurjchem.com:article/775" metadataPrefix="oai_dc" verb="GetRecord">https://www.eurjchem.com/index.php/eurjchem/oai</request>
	<GetRecord>
		<record>
			<header>
				<identifier>oai:ojs.www.eurjchem.com:article/775</identifier>
				<datestamp>2013-12-31T06:16:57Z</datestamp>
				<setSpec>eurjchem:REW</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">The chemical reactivity of naphthols and their derivatives toward α-cyanocinnamonitriles and ethyl α-cyanocinnamates: A review of synthesis, reactions and applications of naphthopyrano</dc:title>
	<dc:creator>El-Wahab, Ashraf Hassan Fekry Abd</dc:creator>
	<dc:creator>Mohamed, Hany Mostafa</dc:creator>
	<dc:creator>El-Agrody, Ahmed Mohamed</dc:creator>
	<dc:creator>Bedair, Ahmed Hammam</dc:creator>
	<dc:subject xml:lang="en-US">Naphthols</dc:subject>
	<dc:subject xml:lang="en-US">Naphthopyran</dc:subject>
	<dc:subject xml:lang="en-US">Nucleophilic reagents</dc:subject>
	<dc:subject xml:lang="en-US">α-Cyanocinnamonitrile</dc:subject>
	<dc:subject xml:lang="en-US">Naphthopyranopyrimidine</dc:subject>
	<dc:subject xml:lang="en-US">Naphthopyranotriazolopyrimidine</dc:subject>
	<dc:description xml:lang="en-US">This review deals with synthesis and reactions of some naphthopyrano derivatives and their applications. The main purpose of this review is to present a survey of literatures on the reactivity of naphthols and their derivatives toward α-cyanocinnamonitrile or ethyl α-cyanocinnamate derivatives and the reactions of β-enaminonitriles and β-enaminoesters with different electrophiles followed by nucleophilic reagents. Some of these reactions have been applied successfully to the synthesis of biologically important compounds.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2013-12-31</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/775</dc:identifier>
	<dc:identifier>10.5155/eurjchem.4.4.467-483.775</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 4 No. 4 (2013): December 2013; 467-483</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/775/PDF</dc:relation>
</oai_dc:dc>
			</metadata>
		</record>
	</GetRecord>
</OAI-PMH>
