<?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>2026-05-12T19:22:29Z</responseDate>
	<request identifier="oai:ojs.www.eurjchem.com:article/610" metadataPrefix="oai_dc" verb="GetRecord">https://www.eurjchem.com/index.php/eurjchem/oai</request>
	<GetRecord>
		<record>
			<header>
				<identifier>oai:ojs.www.eurjchem.com:article/610</identifier>
				<datestamp>2012-12-31T23:10:35Z</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">Efficient deprotection of Boc group in amines and sulfamides  using Dawson heteropolyacid catalyst</dc:title>
	<dc:creator>Belghiche, Roubila</dc:creator>
	<dc:creator>Cheraiet, Zinelaabidine</dc:creator>
	<dc:creator>Berredjem, Malika</dc:creator>
	<dc:creator>Abbessi, Mostefa</dc:creator>
	<dc:creator>Aouf, Nour-Eddine</dc:creator>
	<dc:subject xml:lang="en-US">Catalyst</dc:subject>
	<dc:subject xml:lang="en-US">Cyclosulfamides</dc:subject>
	<dc:subject xml:lang="en-US">Protective group</dc:subject>
	<dc:subject xml:lang="en-US">N-Boc deprotection</dc:subject>
	<dc:subject xml:lang="en-US">Dawson heteropolyacid</dc:subject>
	<dc:subject xml:lang="en-US">Heterogeneous catalysis</dc:subject>
	<dc:description xml:lang="en-US">A series of sulfamides containing two protecting groups have been synthesized starting from N-benzoylaminoacids derivatives of (glycine, alanine, valine, leucine, phenylalanine), chlorosulfonylisocyanate and primary amines. Selective deprotection of the cyclic or linear sulfamides and amines has been achieved by treatment with heteropolyacid, which is easily recoverable and reusable. This method represents a reasonable alternative to the previous reported deprotection procedures.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2012-09-30</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/610</dc:identifier>
	<dc:identifier>10.5155/eurjchem.3.3.305-309.610</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 3 No. 3 (2012): September 2012; 305-309</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/610/PDF</dc:relation>
</oai_dc:dc>
			</metadata>
		</record>
	</GetRecord>
</OAI-PMH>
