@proceedings {7692,
	title = {Effet d\&rsquo;administration du chlorure de nickel associ{\'e} avec le s{\'e}l{\'e}nium sur les param{\`e}tres h{\'e}matologiques et la glande surr{\'e}nale chez le rat wistar },
	journal = {XII{\`e}me Journ{\'e}es de Pharmacie et VII{\`e}me Journ{\'e}es de la Douleur 04 et 05 Juin },
	year = {2014},
	address = {Batna, Alg{\'e}rie},
	author = {BOULIA ISMAHENE and Ounassa Adjroud}
}
@article {MEZAACHE20147167,
	title = {Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion},
	journal = {Tetrahedron Letters},
	volume = {55},
	number = {52},
	year = {2014},
	pages = {7167-7171},
	abstract = {
	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.

},
	keywords = {Acetal, Alcohol, Bis(methoxyphenyl)methyl, Copper, Protecting group, Transprotection},
	issn = {0040-4039},
	doi = {https://doi.org/10.1016/j.tetlet.2014.10.115},
	url = {https://www.sciencedirect.com/science/article/pii/S0040403914018218},
	author = {RofiaMezaache and Hassina Harkat and Julie Obszynski and Abdelhamid Benkouider and Aur{\'e}lien Blanc and Jean-Marc Weibel and Patrick Pale}
}
@article {article,
	title = {ChemInform Abstract: Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides.},
	journal = {Advanced Synthesis \& Catalysis},
	volume = {356},
	number = {18},
	year = {2014},
	month = {12},
	pages = {3842-3848},
	abstract = {
	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\&nbsp;N-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\&nbsp;0.8 mol\%\&nbsp;of this heterogeneous copper catalyst still gave good conversion and yields.



	\&nbsp;



	
		\&nbsp;
	



	

},
	doi = {10.1002/adsc.201400189},
	url = {https://onlinelibrary.wiley.com/doi/10.1002/adsc.201400189},
	author = {Hassina Harkat and Sophie Borgh{\`e}se and Nigris, Matteo and Serguei Kiselev and Val{\'e}rie B{\'e}n{\'e}teau and Patrick Pale}
}
@proceedings {6319,
	title = {Mild, efficient derivatives indole synthesis using USY-CuI zeolite as a reusable catalyst},
	journal = {XII {\`e}mes journees de pharmacie et VII eme journee de lutte contre la douleur 04 et 05 Juin },
	year = {2014},
	address = {Batna, Alg{\'e}rie},
	author = {HARKAT Hassina}
}
@proceedings {6318,
	title = {An efficient and reusable catalyst for Von Pechmann reaction},
	journal = {Sciences d{\textquoteright}Interfaces Chimie {\textendash} Biologie SNSI C-B, 22 et 23 Octobre},
	year = {2014},
	address = {Souk Ahras, Alg{\'e}rie},
	author = {HARKAT Hassina}
}
@proceedings {6315,
	title = {LES MOLECULES BIOACTIVES ET L\&$\#$39;ACTIVITE BIOLOGIQUE DE LA PLANTE BASSIA MURICATA},
	journal = {XII {\`e}mes journees de pharmacie et VII eme journee de lutte contre la douleur 04 et 05 Juin },
	year = {2014},
	address = {Batna, Alg{\'e}rie},
	author = {BOUZGHAIA Badra}
}
@proceedings {6313,
	title = {Synthesis of 1,4- dihydropyridines through Hantzsch reaction catalyzed by p- toluenesulfonate complexes of copper (II)},
	journal = {Sciences d{\textquoteright}Interfaces Chimie {\textendash} Biologie SNSI C-B, 22 et 23 Octobre },
	year = {2014},
	address = {Souk Ahras, Alg{\'e}rie},
	author = {Zouchoune Soria}
}
@proceedings {6308,
	title = {Sythesis and structural study of hydrogen neodymium sulfate tetrahydrate},
	journal = {4{\`e}me Colloque International de Chimie CIC-4, Batna, 25 -27 Novembre },
	year = {2014},
	address = {Batna, Alg{\'e}rie},
	author = {BENSADEK Ali}
}
@proceedings {6299,
	title = {ETUDE PHYTOCHIMIQUE DE L\&$\#$39;ESPESE BASSIA MURICATA ET LEUR ACTIVITE BIOLOGIQUE},
	journal = {4{\`e}me Colloque International de Chimie CIC-4, Batna, 25 -27 Novembre },
	year = {2014},
	address = {Batna, Alg{\'e}rie},
	author = {BOUZGHAIA Badra}
}
@proceedings {6297,
	title = {SYNTHESES DES HETEROCYCLES AZOTES : 1,4DIHYDRO-PYRIDINE CATALYSEE PAR TOSYLATE DE CUIVRE},
	journal = {4{\`e}me Colloque International de Chimie CIC-4, Batna, 25 -27 Novembre },
	year = {2014},
	address = {Batna, Alg{\'e}rie},
	author = {Zouchoune Soria}
}
@proceedings {6287,
	title = {Effet d\&rsquo;administration du chlorure de nickel associ{\'e} avec le s{\'e}l{\'e}nium sur les param{\`e}tres h{\'e}matologiques et la glande surr{\'e}nale chez le rat wistar},
	journal = {XII{\`e}me journ{\'e}es de pharmacie et VII{\`e}me journ{\'e}es de la douleur 04 et 05 juin },
	year = {2014},
	address = {Batna, Alg{\'e}rie},
	author = {BOULIA ISMAHENE}
}
@proceedings {6271,
	title = {Influence de la vapeur de gazoline sur la modulation de certaines proteines pulmonaires chez le rat blanc.},
	journal = {First International Congress of Biotoxicologie and Bioactivity, 26 and 27 November},
	year = {2014},
	address = {University of Oran 1, Algeria, },
	author = {Ounassa Adjroud}
}
@proceedings {6270,
	title = {Nephroprotective Effects of Selenium against Nickel Chloride-Induced Nephrotoxicity in Pregnant Rats},
	journal = {ICNSE 2014: April 4-5, },
	year = {2014},
	address = {Dubai, UAE},
	author = {Ounassa Adjroud}
}
@article {6243,
	title = {Inventaire et dynamique globale du peuplement des n{\'e}matodes phytoparasites (Nematoda : Secernentea) de l\&rsquo;olivier (Olea europeae) dans une r{\'e}gion aride du Nord-Est de l\&rsquo;Alg{\'e}rie},
	journal = {Journal of Animal \&Plant Sciences},
	volume = {23},
	number = {3},
	year = {2014},
	pages = {3637-3645 },
	abstract = {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, Fronto{\"\i} and S{\'e}villane. 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\&nbsp;Aphelenchida represent only 7.15\%. The genus Pratylenchus records alone 54.75\% on the S{\'e}villane 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 S{\'e}villane 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.},
	author = {Smail Chafaa and Abdelkrim SI-BACHIR and Meriem BOUKHADRA and Asma ACHI}
}
@article {6234,
	title = {Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion},
	journal = {Tetrahedron Letters},
	volume = {55},
	number = {52},
	year = {2014},
	pages = {7167-7171},
	abstract = {
	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.

},
	author = {RofiaMezaache and Hassina Harkat and Julie Obszynski and Abdelhamid Benkouider and Aur{\'e}lien Blanc and Jean-Marc Weibel and Patrick Pale}
}
@article {6231,
	title = {Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides},
	journal = {ADV SYNTH CATAL},
	volume = {356},
	number = {18},
	year = {2014},
	pages = {3842-3848},
	abstract = {
	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\&nbsp;N-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\&nbsp;0.8 mol\%\&nbsp;of this heterogeneous copper catalyst still gave good conversion and yields.



	\&nbsp;



	
		\&nbsp;
	

},
	author = {Hassina Harkat and Sophie Borgh{\`e}se and Matteo De Nigris and Serguei Kiselev and Val{\'e}rie B{\'e}n{\'e}teau and Patrick Pale}
}
