2014
Mahdavi A, Bahloul A, Haghighat F, Ostiguy C.
Contribution of breathing frequency and inhalation flow rate on performance of N95 filtering facepiece respirators. Annals of occupational hygieneAnnals of Occupational Hygiene. 2014;58 :195-205.
Boubaker L, Djebabra MEBAREK, Saadi S.
Contribution of stakeholder theory in the management of environmental quality of Algerian firms: case study of the SONATRACH group, Algeria. Management of Environmental Quality: An International JournalManagement of Environmental Quality: An International Journal. 2014.
Boubaker L, Djebabra MEBAREK, Saadi S.
Contribution of stakeholder theory in the management of environmental quality of Algerian firms: case study of the SONATRACH group, Algeria. Management of Environmental Quality: An International JournalManagement of Environmental Quality: An International Journal. 2014.
Boubaker L, Djebabra MEBAREK, Saadi S.
Contribution of stakeholder theory in the management of environmental quality of Algerian firms: case study of the SONATRACH group, Algeria. Management of Environmental Quality: An International JournalManagement of Environmental Quality: An International Journal. 2014.
Tir Z, Radjeai H, Abdessemed R.
Control of a wind energy conversion system based on brushless doubly fed induction generator. Revue des Energies RenouvelablesRevue des Energies Renouvelables. 2014;17.
Tir Z, Radjeai H, Abdessemed R.
Control of a wind energy conversion system based on brushless doubly fed induction generator. Revue des Energies RenouvelablesRevue des Energies Renouvelables. 2014;17.
Tir Z, Radjeai H, Abdessemed R.
Control of a wind energy conversion system based on brushless doubly fed induction generator. Revue des Energies RenouvelablesRevue des Energies Renouvelables. 2014;17.
RofiaMezaache, Harkat H, Obszynski J, Benkouider A, Blanc A, Weibel J-M, Pale P.
Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion. Tetrahedron LettersTetrahedron Letters. 2014;55 :7167-7171.
AbstractTransprotection 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.
RofiaMezaache, Harkat H, Obszynski J, Benkouider A, Blanc A, Weibel J-M, Pale P.
Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion. Tetrahedron LettersTetrahedron Letters. 2014;55 :7167-7171.
AbstractTransprotection 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.
RofiaMezaache, Harkat H, Obszynski J, Benkouider A, Blanc A, Weibel J-M, Pale P.
Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion. Tetrahedron LettersTetrahedron Letters. 2014;55 :7167-7171.
AbstractTransprotection 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.
RofiaMezaache, Harkat H, Obszynski J, Benkouider A, Blanc A, Weibel J-M, Pale P.
Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion. Tetrahedron LettersTetrahedron Letters. 2014;55 :7167-7171.
AbstractTransprotection 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.
RofiaMezaache, Harkat H, Obszynski J, Benkouider A, Blanc A, Weibel J-M, Pale P.
Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion. Tetrahedron LettersTetrahedron Letters. 2014;55 :7167-7171.
AbstractTransprotection 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.
RofiaMezaache, Harkat H, Obszynski J, Benkouider A, Blanc A, Weibel J-M, Pale P.
Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion. Tetrahedron LettersTetrahedron Letters. 2014;55 :7167-7171.
AbstractTransprotection 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.
RofiaMezaache, Harkat H, Obszynski J, Benkouider A, Blanc A, Weibel J-M, Pale P.
Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion. Tetrahedron LettersTetrahedron Letters. 2014;55 :7167-7171.
AbstractTransprotection 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.