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2011
H B, Asma R. Contribution à l’étude géotechnique du barrage Yabous –Khenchela. Univ de Batna. 2011.
Khamari D, Makouf A, Drid S. Control of induction motor using polytopic LPV models. 2011 International Conference on Communications, Computing and Control Applications (CCCA). 2011 :1-5.
Khamari D, Makouf A, Drid S. Control of induction motor using polytopic LPV models. 2011 International Conference on Communications, Computing and Control Applications (CCCA). 2011 :1-5.
Khamari D, Makouf A, Drid S. Control of induction motor using polytopic LPV models. 2011 International Conference on Communications, Computing and Control Applications (CCCA). 2011 :1-5.
BOUGOFFA LAZHAR, Rach RC, MENNOUNI ABDELAZIZ. A convenient technique for solving linear and nonlinear Abel integral equations by the Adomian decomposition method. Applied Mathematics and ComputationApplied Mathematics and Computation. 2011;218 :1785-1793.
BOUGOFFA LAZHAR, Rach RC, MENNOUNI ABDELAZIZ. A convenient technique for solving linear and nonlinear Abel integral equations by the Adomian decomposition method. Applied Mathematics and ComputationApplied Mathematics and Computation. 2011;218 :1785-1793.
BOUGOFFA LAZHAR, Rach RC, MENNOUNI ABDELAZIZ. A convenient technique for solving linear and nonlinear Abel integral equations by the Adomian decomposition method. Applied Mathematics and ComputationApplied Mathematics and Computation. 2011;218 :1785-1793.
Specklin S, Gallier F, Mezaache R, Harkat H, Yénimégué A, Weibel J-M, Blanc A, Pale P. Copper(II) Bromide as Efficient Catalyst for Silyl- to Bisarylmethyl Ethers Interconversion (Transprotection). Tetrahedron LettersTetrahedron Letters. 2011;52 :5820-5823.Abstract
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process. Graphical abstract Primary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Specklin S, Gallier F, Mezaache R, Harkat H, Yénimégué A, Weibel J-M, Blanc A, Pale P. Copper(II) Bromide as Efficient Catalyst for Silyl- to Bisarylmethyl Ethers Interconversion (Transprotection). Tetrahedron LettersTetrahedron Letters. 2011;52 :5820-5823.Abstract
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process. Graphical abstract Primary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Specklin S, Gallier F, Mezaache R, Harkat H, Yénimégué A, Weibel J-M, Blanc A, Pale P. Copper(II) Bromide as Efficient Catalyst for Silyl- to Bisarylmethyl Ethers Interconversion (Transprotection). Tetrahedron LettersTetrahedron Letters. 2011;52 :5820-5823.Abstract
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process. Graphical abstract Primary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Specklin S, Gallier F, Mezaache R, Harkat H, Yénimégué A, Weibel J-M, Blanc A, Pale P. Copper(II) Bromide as Efficient Catalyst for Silyl- to Bisarylmethyl Ethers Interconversion (Transprotection). Tetrahedron LettersTetrahedron Letters. 2011;52 :5820-5823.Abstract
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process. Graphical abstract Primary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Specklin S, Gallier F, Mezaache R, Harkat H, Yénimégué A, Weibel J-M, Blanc A, Pale P. Copper(II) Bromide as Efficient Catalyst for Silyl- to Bisarylmethyl Ethers Interconversion (Transprotection). Tetrahedron LettersTetrahedron Letters. 2011;52 :5820-5823.Abstract
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process. Graphical abstract Primary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Specklin S, Gallier F, Mezaache R, Harkat H, Yénimégué A, Weibel J-M, Blanc A, Pale P. Copper(II) Bromide as Efficient Catalyst for Silyl- to Bisarylmethyl Ethers Interconversion (Transprotection). Tetrahedron LettersTetrahedron Letters. 2011;52 :5820-5823.Abstract
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process. Graphical abstract Primary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Specklin S, Gallier F, Mezaache R, Harkat H, Yénimégué A, Weibel J-M, Blanc A, Pale P. Copper(II) Bromide as Efficient Catalyst for Silyl- to Bisarylmethyl Ethers Interconversion (Transprotection). Tetrahedron LettersTetrahedron Letters. 2011;52 :5820-5823.Abstract
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process. Graphical abstract Primary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Specklin S, Gallier F, Mezaache R, Harkat H, Yénimégué A, Weibel J-M, Blanc A, Pale P. Copper(II) Bromide as Efficient Catalyst for Silyl- to Bisarylmethyl Ethers Interconversion (Transprotection). Tetrahedron LettersTetrahedron Letters. 2011;52 :5820-5823.Abstract
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process. Graphical abstract Primary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Mebarki G, Rebay M, RAHAL S. Couplage conduction-convection en régime transitoire. CFM 2011-20ème Congrès Français de Mécanique. 2011.
Mebarki G, Rebay M, RAHAL S. Couplage conduction-convection en regime transitoire.; 2011.
Mebarki G, Rebay M, RAHAL S. Couplage conduction-convection en régime transitoire. CFM 2011-20ème Congrès Français de Mécanique. 2011.
Mebarki G, Rebay M, RAHAL S. Couplage conduction-convection en regime transitoire.; 2011.
Mebarki G, Rebay M, RAHAL S. Couplage conduction-convection en regime transitoire.; 2011.

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