<?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>2026-04-14T22:19:29Z</responseDate>
	<request identifier="oai:ojs.www.eurjchem.com:article/1477" metadataPrefix="oai_dc" verb="GetRecord">https://www.eurjchem.com/index.php/eurjchem/oai</request>
	<GetRecord>
		<record>
			<header>
				<identifier>oai:ojs.www.eurjchem.com:article/1477</identifier>
				<datestamp>2016-12-31T08:51:22Z</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">Eaton’s reagent catalysed alacritous synthesis of 3-benzazepinones</dc:title>
	<dc:creator>Thimmaiah, Shubhavathi</dc:creator>
	<dc:creator>Ningegowda, Mallesha</dc:creator>
	<dc:creator>Shivananju, Nanjunda Swamy</dc:creator>
	<dc:creator>Ningegowda, Raghu</dc:creator>
	<dc:creator>Siddaraj, Ranjith</dc:creator>
	<dc:creator>Priya, Babu Shubha</dc:creator>
	<dc:subject xml:lang="en-US">Alacritous</dc:subject>
	<dc:subject xml:lang="en-US">Eaton’s reagent</dc:subject>
	<dc:subject xml:lang="en-US">3-Benzazepinone</dc:subject>
	<dc:subject xml:lang="en-US">Solvent free reaction</dc:subject>
	<dc:subject xml:lang="en-US">Methane sulfonic acid</dc:subject>
	<dc:subject xml:lang="en-US">Phosphorous pentoxide</dc:subject>
	<dc:description xml:lang="en-US">An expeditious method for the synthesis of 3-benzazepinones has been developed by using a mixture of phosphorus pentoxide-methane sulfonic acid (Eaton’s reagent) at room temperature under solvent and metal catalyst free condition. Wide functional group tolerance, mild reaction conditions, simple procedure, ease of work-up and high yields is the citable features of this protocol.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2016-12-31</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/1477</dc:identifier>
	<dc:identifier>10.5155/eurjchem.7.4.391-396.1477</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 7 No. 4 (2016): December 2016; 391-396</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/1477/pdf_1477</dc:relation>
</oai_dc:dc>
			</metadata>
		</record>
	</GetRecord>
</OAI-PMH>
