<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">BOULIA ISMAHENE</style></author><author><style face="normal" font="default" size="100%">Ounassa Adjroud</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effet d&amp;rsquo;administration du chlorure de nickel associé avec le sélénium sur les paramètres hématologiques et la glande surrénale chez le rat wistar </style></title><secondary-title><style face="normal" font="default" size="100%">XIIème Journées de Pharmacie et VIIème Journées de la Douleur 04 et 05 Juin </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Batna, Algérie</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">RofiaMezaache</style></author><author><style face="normal" font="default" size="100%">Hassina Harkat</style></author><author><style face="normal" font="default" size="100%">Julie Obszynski</style></author><author><style face="normal" font="default" size="100%">Abdelhamid Benkouider</style></author><author><style face="normal" font="default" size="100%">Aurélien Blanc</style></author><author><style face="normal" font="default" size="100%">Jean-Marc Weibel</style></author><author><style face="normal" font="default" size="100%">Patrick Pale</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion</style></title><secondary-title><style face="normal" font="default" size="100%">Tetrahedron Letters</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acetal</style></keyword><keyword><style  face="normal" font="default" size="100%">Alcohol</style></keyword><keyword><style  face="normal" font="default" size="100%">Bis(methoxyphenyl)methyl</style></keyword><keyword><style  face="normal" font="default" size="100%">Copper</style></keyword><keyword><style  face="normal" font="default" size="100%">Protecting group</style></keyword><keyword><style  face="normal" font="default" size="100%">Transprotection</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0040403914018218</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">55</style></volume><pages><style face="normal" font="default" size="100%">7167-7171</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;
	Transprotection of acetals to bis(methoxyphenyl)methyl (BMPM) ethers can be efficiently achieved in the presence of copper dibromide as catalyst in acetonitrile at room temperature. Acetals are conveniently and selectively converted to the corresponding mono-protected diol with bis(methoxyphenyl)methyl isopropyl ether (BMPMOiPr) as the reagent. This new practical reagent allows the BMPM transfer to 1,3-dioxolanes or 1,3-dioxanes under copper catalysis. The reaction conditions are also very mild and tolerant to various functional groups, including other protecting groups.
&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">52</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hassina Harkat</style></author><author><style face="normal" font="default" size="100%">Sophie Borghèse</style></author><author><style face="normal" font="default" size="100%">Nigris, Matteo</style></author><author><style face="normal" font="default" size="100%">Serguei Kiselev</style></author><author><style face="normal" font="default" size="100%">Valérie Bénéteau</style></author><author><style face="normal" font="default" size="100%">Patrick Pale</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ChemInform Abstract: Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides.</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Synthesis &amp; Catalysis</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">12</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/10.1002/adsc.201400189</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">356</style></volume><pages><style face="normal" font="default" size="100%">3842-3848</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;
	Copper(I)-zeolites, especially copper(I)-ultra stable Y zeolite (USY), are very efficient heterogeneous catalysts for the coupling of functionalized 1-bromoalkynes and various nitrogen derivatives. Under these conditions, sulfonylated alkyl- or arylamines and various N-heterocycles, such as oxazolidinones or indoles, could be efficiently transformed into the corresponding&amp;nbsp;&lt;i&gt;N&lt;/i&gt;-alkynyl derivatives. However, imidazoles gave addition products rather than coupling products. The reaction conditions proved compatible with a variety of functional and protecting groups. Such zeolitic catalysts can be recycled and reused at least five times without significant deactivation. Low catalyst loading could be used (4 mol%) and as low as&amp;nbsp;&lt;i&gt;0.8 mol%&lt;/i&gt;&amp;nbsp;of this heterogeneous copper catalyst still gave good conversion and yields.
&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;
	&amp;nbsp;
&lt;/p&gt;

&lt;figure&gt;
	&lt;p style=&quot;text-align: justify;&quot;&gt;
		&amp;nbsp;
	&lt;/p&gt;
&lt;/figure&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;
	&lt;a href=&quot;https://onlinelibrary.wiley.com/cms/asset/eeb06caa-463b-49ed-b08e-81c7bc1d1d59/mcontent.jpg&quot; target=&quot;_blank&quot;&gt;&lt;img alt=&quot;image&quot; data-lg-src=&quot;/cms/asset/eeb06caa-463b-49ed-b08e-81c7bc1d1d59/mcontent.jpg&quot; loading=&quot;lazy&quot; src=&quot;https://onlinelibrary.wiley.com/cms/asset/0a7ef62a-c89a-4034-a7dd-1c736bd3a478/mcontent.gif&quot;&gt;&lt;/a&gt;
&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">18</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">HARKAT Hassina</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mild, efficient derivatives indole synthesis using USY-CuI zeolite as a reusable catalyst</style></title><secondary-title><style face="normal" font="default" size="100%">XII èmes journees de pharmacie et VII eme journee de lutte contre la douleur 04 et 05 Juin </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Batna, Algérie</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">HARKAT Hassina</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">An efficient and reusable catalyst for Von Pechmann reaction</style></title><secondary-title><style face="normal" font="default" size="100%">Sciences d’Interfaces Chimie – Biologie SNSI C-B, 22 et 23 Octobre</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Souk Ahras, Algérie</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">BOUZGHAIA Badra</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">LES MOLECULES BIOACTIVES ET L&amp;#39;ACTIVITE BIOLOGIQUE DE LA PLANTE BASSIA MURICATA</style></title><secondary-title><style face="normal" font="default" size="100%">XII èmes journees de pharmacie et VII eme journee de lutte contre la douleur 04 et 05 Juin </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Batna, Algérie</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zouchoune Soria</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis of 1,4- dihydropyridines through Hantzsch reaction catalyzed by p- toluenesulfonate complexes of copper (II)</style></title><secondary-title><style face="normal" font="default" size="100%">Sciences d’Interfaces Chimie – Biologie SNSI C-B, 22 et 23 Octobre </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Souk Ahras, Algérie</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">BENSADEK Ali</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sythesis and structural study of hydrogen neodymium sulfate tetrahydrate</style></title><secondary-title><style face="normal" font="default" size="100%">4ème Colloque International de Chimie CIC-4, Batna, 25 -27 Novembre </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Batna, Algérie</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">BOUZGHAIA Badra</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ETUDE PHYTOCHIMIQUE DE L&amp;#39;ESPESE BASSIA MURICATA ET LEUR ACTIVITE BIOLOGIQUE</style></title><secondary-title><style face="normal" font="default" size="100%">4ème Colloque International de Chimie CIC-4, Batna, 25 -27 Novembre </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Batna, Algérie</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zouchoune Soria</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">SYNTHESES DES HETEROCYCLES AZOTES : 1,4DIHYDRO-PYRIDINE CATALYSEE PAR TOSYLATE DE CUIVRE</style></title><secondary-title><style face="normal" font="default" size="100%">4ème Colloque International de Chimie CIC-4, Batna, 25 -27 Novembre </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Batna, Algérie</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">BOULIA ISMAHENE</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effet d&amp;rsquo;administration du chlorure de nickel associé avec le sélénium sur les paramètres hématologiques et la glande surrénale chez le rat wistar</style></title><secondary-title><style face="normal" font="default" size="100%">XIIème journées de pharmacie et VIIème journées de la douleur 04 et 05 juin </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Batna, Algérie</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ounassa Adjroud</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence de la vapeur de gazoline sur la modulation de certaines proteines pulmonaires chez le rat blanc.</style></title><secondary-title><style face="normal" font="default" size="100%">First International Congress of Biotoxicologie and Bioactivity, 26 and 27 November</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">University of Oran 1, Algeria, </style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ounassa Adjroud</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nephroprotective Effects of Selenium against Nickel Chloride-Induced Nephrotoxicity in Pregnant Rats</style></title><secondary-title><style face="normal" font="default" size="100%">ICNSE 2014: April 4-5, </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Dubai, UAE</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Smail Chafaa</style></author><author><style face="normal" font="default" size="100%">Abdelkrim SI-BACHIR</style></author><author><style face="normal" font="default" size="100%">Meriem BOUKHADRA</style></author><author><style face="normal" font="default" size="100%">Asma ACHI</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inventaire et dynamique globale du peuplement des nématodes phytoparasites (Nematoda : Secernentea) de l&amp;rsquo;olivier (Olea europeae) dans une région aride du Nord-Est de l&amp;rsquo;Algérie</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Animal &amp;Plant Sciences</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><volume><style face="normal" font="default" size="100%">23</style></volume><pages><style face="normal" font="default" size="100%">3637-3645 </style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The community of nematodes (Nematoda: Secernentea) in groves of North East Algeria, has been the subject of regular observations of September 2011 to May 2012. Sampling and extraction of nematodes by the buckets technique are conducted following the method of Baermann. The sampling groves are composed by olive trees (Olea europea: Oleaceae) from four varieties: Chemlal, Sigoise, Frontoï and Sévillane. We identified a total of 531 individuals. The systematic inventory revealed 14 genus of Nematoda, belonging to 10 families and 3 orders. The Tylenchida and Dorylaimida are the best represented orders. They represent 92.85% of the total community of all identified nematodes, while&amp;nbsp;Aphelenchida represent only 7.15%. The genus Pratylenchus records alone 54.75% on the Sévillane variety and 33.02% on the Frantoi variety. The most represented genus on Sigoise and Chemlal varieties is Meloidogyne with respectively 43.24% and 30.43%. Grove of Sévillane variety hosts the highest abundance of nematodes with 57.44%; against only 19.96%, 13.94% and 8.66%, respectively, for the varieties Frantoi, Sigoise and Chemlal. Depending on the seasons, nematodes are more abundant in autumn (88.52%) than in winter (8.66%) and the spring (2.82%). Pratylenchus and Meloidogyne are noted with large numbers, especially in winter.</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">RofiaMezaache</style></author><author><style face="normal" font="default" size="100%">Hassina Harkat</style></author><author><style face="normal" font="default" size="100%">Julie Obszynski</style></author><author><style face="normal" font="default" size="100%">Abdelhamid Benkouider</style></author><author><style face="normal" font="default" size="100%">Aurélien Blanc</style></author><author><style face="normal" font="default" size="100%">Jean-Marc Weibel</style></author><author><style face="normal" font="default" size="100%">Patrick Pale</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion</style></title><secondary-title><style face="normal" font="default" size="100%">Tetrahedron Letters</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><volume><style face="normal" font="default" size="100%">55</style></volume><pages><style face="normal" font="default" size="100%">7167-7171</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;
	Transprotection of acetals to bis(methoxyphenyl)methyl (BMPM) ethers can be efficiently achieved in the presence of copper dibromide as catalyst in acetonitrile at room temperature. Acetals are conveniently and selectively converted to the corresponding mono-protected diol with bis(methoxyphenyl)methyl isopropyl ether (BMPMO&lt;em&gt;i&lt;/em&gt;Pr) as the reagent. This new practical reagent allows the BMPM transfer to 1,3-dioxolanes or 1,3-dioxanes under copper catalysis. The reaction conditions are also very mild and tolerant to various functional groups, including other protecting groups.
&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">52</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hassina Harkat</style></author><author><style face="normal" font="default" size="100%">Sophie Borghèse</style></author><author><style face="normal" font="default" size="100%">Matteo De Nigris</style></author><author><style face="normal" font="default" size="100%">Serguei Kiselev</style></author><author><style face="normal" font="default" size="100%">Valérie Bénéteau</style></author><author><style face="normal" font="default" size="100%">Patrick Pale</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides</style></title><secondary-title><style face="normal" font="default" size="100%">ADV SYNTH CATAL</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><volume><style face="normal" font="default" size="100%">356</style></volume><pages><style face="normal" font="default" size="100%">3842-3848</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;
	Copper(I)-zeolites, especially copper(I)-ultra stable Y zeolite (USY), are very efficient heterogeneous catalysts for the coupling of functionalized 1-bromoalkynes and various nitrogen derivatives. Under these conditions, sulfonylated alkyl- or arylamines and various N-heterocycles, such as oxazolidinones or indoles, could be efficiently transformed into the corresponding&amp;nbsp;&lt;i&gt;N&lt;/i&gt;-alkynyl derivatives. However, imidazoles gave addition products rather than coupling products. The reaction conditions proved compatible with a variety of functional and protecting groups. Such zeolitic catalysts can be recycled and reused at least five times without significant deactivation. Low catalyst loading could be used (4 mol%) and as low as&amp;nbsp;&lt;i&gt;0.8 mol%&lt;/i&gt;&amp;nbsp;of this heterogeneous copper catalyst still gave good conversion and yields.
&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;
	&amp;nbsp;
&lt;/p&gt;

&lt;figure&gt;
	&lt;p style=&quot;text-align: justify;&quot;&gt;
		&amp;nbsp;
	&lt;/p&gt;
&lt;/figure&gt;
&lt;a href=&quot;https://onlinelibrary.wiley.com/cms/asset/eeb06caa-463b-49ed-b08e-81c7bc1d1d59/mcontent.jpg&quot; target=&quot;_blank&quot;&gt;&lt;img alt=&quot;image&quot; data-lg-src=&quot;/cms/asset/eeb06caa-463b-49ed-b08e-81c7bc1d1d59/mcontent.jpg&quot; loading=&quot;lazy&quot; src=&quot;https://onlinelibrary.wiley.com/cms/asset/0a7ef62a-c89a-4034-a7dd-1c736bd3a478/mcontent.gif&quot; title=&quot;image&quot;&gt;&lt;/a&gt;</style></abstract><issue><style face="normal" font="default" size="100%">18</style></issue></record></records></xml>