Publications

2014
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Abu-Odeh M, Bar-Mag T, Huang H, Kim TH, Salah Z, Abdeen SK, Sudol M, Reichmann D, Sidhu S, Kim PM. Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks. Journal of Biological ChemistryJournal of Biological Chemistry. 2014;289 :8865-8880.
Harkat H, Borghèse S, Nigris M, Kiselev S, Bénéteau V, Pale P. ChemInform Abstract: Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. Advanced Synthesis & CatalysisAdvanced Synthesis & Catalysis. 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 M, Kiselev S, Bénéteau V, Pale P. ChemInform Abstract: Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. Advanced Synthesis & CatalysisAdvanced Synthesis & Catalysis. 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 M, Kiselev S, Bénéteau V, Pale P. ChemInform Abstract: Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. Advanced Synthesis & CatalysisAdvanced Synthesis & Catalysis. 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 M, Kiselev S, Bénéteau V, Pale P. ChemInform Abstract: Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. Advanced Synthesis & CatalysisAdvanced Synthesis & Catalysis. 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 M, Kiselev S, Bénéteau V, Pale P. ChemInform Abstract: Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. Advanced Synthesis & CatalysisAdvanced Synthesis & Catalysis. 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 M, Kiselev S, Bénéteau V, Pale P. ChemInform Abstract: Zeo-Click Synthesis: Copper-Zeolite-Catalyzed Synthesis of Ynamides. Advanced Synthesis & CatalysisAdvanced Synthesis & Catalysis. 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.    
Abid M, Mansouri MA, Ouragui S. Chirurgie du cancer colorectal par laparoscopie chez les sujets de plus de 70 ans. Expérience de la Clinique Debussy.; 2014.
Abid M, Mansouri MA, Ouragui S. Chirurgie du cancer colorectal par laparoscopie chez les sujets de plus de 70 ans. Expérience de la Clinique Debussy.; 2014.
Abid M, Mansouri MA, Ouragui S. Chirurgie du cancer colorectal par laparoscopie chez les sujets de plus de 70 ans. Expérience de la Clinique Debussy.; 2014.
Goual HAFIDA, Seddik-Ameur N. Chi-squared type test for the AFT-generalized inverse Weibull distribution. Communications in statistics-Theory and MethodsCommunications in statistics-Theory and Methods. 2014;43 :2605-2617.

Pages