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.
AbstractCopper(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.
AbstractCopper(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.
AbstractCopper(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.
AbstractCopper(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.
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.
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.
Steiner AL, Tawfik AB, Shalaby A, Zakey AS, Abdel-Wahab MM, Salah Z, Solmon F, Sillman S, Zaveri RA.
Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region. Climate researchClimate research. 2014;59 :207-228.
Steiner AL, Tawfik AB, Shalaby A, Zakey AS, Abdel-Wahab MM, Salah Z, Solmon F, Sillman S, Zaveri RA.
Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region. Climate researchClimate research. 2014;59 :207-228.
Steiner AL, Tawfik AB, Shalaby A, Zakey AS, Abdel-Wahab MM, Salah Z, Solmon F, Sillman S, Zaveri RA.
Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region. Climate researchClimate research. 2014;59 :207-228.
Steiner AL, Tawfik AB, Shalaby A, Zakey AS, Abdel-Wahab MM, Salah Z, Solmon F, Sillman S, Zaveri RA.
Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region. Climate researchClimate research. 2014;59 :207-228.
Steiner AL, Tawfik AB, Shalaby A, Zakey AS, Abdel-Wahab MM, Salah Z, Solmon F, Sillman S, Zaveri RA.
Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region. Climate researchClimate research. 2014;59 :207-228.
Steiner AL, Tawfik AB, Shalaby A, Zakey AS, Abdel-Wahab MM, Salah Z, Solmon F, Sillman S, Zaveri RA.
Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region. Climate researchClimate research. 2014;59 :207-228.
Steiner AL, Tawfik AB, Shalaby A, Zakey AS, Abdel-Wahab MM, Salah Z, Solmon F, Sillman S, Zaveri RA.
Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region. Climate researchClimate research. 2014;59 :207-228.
Steiner AL, Tawfik AB, Shalaby A, Zakey AS, Abdel-Wahab MM, Salah Z, Solmon F, Sillman S, Zaveri RA.
Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region. Climate researchClimate research. 2014;59 :207-228.
Steiner AL, Tawfik AB, Shalaby A, Zakey AS, Abdel-Wahab MM, Salah Z, Solmon F, Sillman S, Zaveri RA.
Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region. Climate researchClimate research. 2014;59 :207-228.
Abid M, Boudissa R, Ourabah A, Hammani A.
Comment Mettre en Place une Réunion de Concertation Pluridisciplinaire (RCP). La Presse Médicale. N°00 JanvierLa Presse Médicale. N°00 Janvier. 2014 :14.