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2014
Bouhata R, KALLA M, Driddi H. use of landsat tm for mapping land use in the endorheic area-case of gadaine plain (eastern Algeria). Annals of the University of Oradea, Geography Series/Analele Universitatii din Oradea, Seria GeografieAnnals of the University of Oradea, Geography Series/Analele Universitatii din Oradea, Seria Geografie. 2014;24.
Bouhata R, KALLA M, Driddi H. use of landsat tm for mapping land use in the endorheic area-case of gadaine plain (eastern Algeria). Annals of the University of Oradea, Geography Series/Analele Universitatii din Oradea, Seria GeografieAnnals of the University of Oradea, Geography Series/Analele Universitatii din Oradea, Seria Geografie. 2014;24.
LAHLOUHI A. Validation of the development methodologies. arXiv preprint arXiv:1408.5511arXiv preprint arXiv:1408.5511. 2014.
Bellala D, SMADI H, Medjghou A. Walk Optimization of a Drilling Operation Carried Out by a Two Link Robot Arm Using Heuristic Approach. International Congress on Energy Efficiency and Energy Related Materials (ENEFM2013). 2014 :51-56.
Bellala D, SMADI H, Medjghou A. Walk Optimization of a Drilling Operation Carried Out by a Two Link Robot Arm Using Heuristic Approach. International Congress on Energy Efficiency and Energy Related Materials (ENEFM2013). 2014 :51-56.
Djamel B. Walk optimization of a drilling operation carried out by a two link robot arm using heuristic approach.; 2014.
Bellala D, SMADI H, Medjghou A. Walk Optimization of a Drilling Operation Carried Out by a Two Link Robot Arm Using Heuristic Approach. International Congress on Energy Efficiency and Energy Related Materials (ENEFM2013). 2014 :51-56.
Necer M, Smail R. Which Yields with Wastes? Study on Pilot of the Efficiency of Water Treatment Plant—Case of the Sector of Algerian Tanning. Journal of Water Resource and ProtectionJournal of Water Resource and Protection. 2014;6 :1457.
Necer M, Smail R. Which Yields with Wastes? Study on Pilot of the Efficiency of Water Treatment Plant—Case of the Sector of Algerian Tanning. Journal of Water Resource and ProtectionJournal of Water Resource and Protection. 2014;6 :1457.
Abu-Odeh M, Salah Z, Herbel C, Hofmann TG, Aqeilan RI. WWOX, the common fragile site FRA16D gene product, regulates ATM activation and the DNA damage response. Proceedings of the National Academy of SciencesProceedings of the National Academy of Sciences. 2014;111 :E4716-E4725.
Abu-Odeh M, Salah Z, Herbel C, Hofmann TG, Aqeilan RI. WWOX, the common fragile site FRA16D gene product, regulates ATM activation and the DNA damage response. Proceedings of the National Academy of SciencesProceedings of the National Academy of Sciences. 2014;111 :E4716-E4725.
Abu-Odeh M, Salah Z, Herbel C, Hofmann TG, Aqeilan RI. WWOX, the common fragile site FRA16D gene product, regulates ATM activation and the DNA damage response. Proceedings of the National Academy of SciencesProceedings of the National Academy of Sciences. 2014;111 :E4716-E4725.
Abu-Odeh M, Salah Z, Herbel C, Hofmann TG, Aqeilan RI. WWOX, the common fragile site FRA16D gene product, regulates ATM activation and the DNA damage response. Proceedings of the National Academy of SciencesProceedings of the National Academy of Sciences. 2014;111 :E4716-E4725.
Abu-Odeh M, Salah Z, Herbel C, Hofmann TG, Aqeilan RI. WWOX, the common fragile site FRA16D gene product, regulates ATM activation and the DNA damage response. Proceedings of the National Academy of SciencesProceedings of the National Academy of Sciences. 2014;111 :E4716-E4725.
Harkat H, Borghèse S, Nigris MD, Kiselev S, Bénéteau V, Pale P. Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. ADV SYNTH CATALADV SYNTH CATAL. 2014;356 :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 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 0.8 mol% of this heterogeneous copper catalyst still gave good conversion and yields.    
Harkat H, Borghèse S, Nigris MD, Kiselev S, Bénéteau V, Pale P. Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. ADV SYNTH CATALADV SYNTH CATAL. 2014;356 :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 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 0.8 mol% of this heterogeneous copper catalyst still gave good conversion and yields.    
Harkat H, Borghèse S, Nigris MD, Kiselev S, Bénéteau V, Pale P. Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. ADV SYNTH CATALADV SYNTH CATAL. 2014;356 :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 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 0.8 mol% of this heterogeneous copper catalyst still gave good conversion and yields.    
Harkat H, Borghèse S, Nigris MD, Kiselev S, Bénéteau V, Pale P. Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. ADV SYNTH CATALADV SYNTH CATAL. 2014;356 :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 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 0.8 mol% of this heterogeneous copper catalyst still gave good conversion and yields.    
Harkat H, Borghèse S, Nigris MD, Kiselev S, Bénéteau V, Pale P. Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. ADV SYNTH CATALADV SYNTH CATAL. 2014;356 :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 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 0.8 mol% of this heterogeneous copper catalyst still gave good conversion and yields.    
Harkat H, Borghèse S, Nigris MD, Kiselev S, Bénéteau V, Pale P. Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. ADV SYNTH CATALADV SYNTH CATAL. 2014;356 :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 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 0.8 mol% of this heterogeneous copper catalyst still gave good conversion and yields.    

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