Institut de Chimie Moléculaire et des Matériaux d'Orsay

Laboratoire de Catalyse Moléculaire - LCM

Mohamed Mellah


Maître de Conférences
Equipe de Catalyse Moléculaire-ICMMO - Bât 420
Université Paris-Sud 11
15, rue Georges Clemenceau
91405 Orsay Cedex
FRANCE

Tél : 01.69.15.47.37
Fax : 01.69.15.46.80
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Publications

Design and electropolymerization of new chiral thiophene–salen
A. Voituriez, M. Mellah and E. Schulz, Synthetic Metals, 156, (2006), 166-175.

Oxidative self-coupling of aromatic compounds in ionic liquids
M. Mellah, J. Zeitouny, S.Gmouh, M. Vaultier and V. Jouikov. Electrochem. Comm. 7(9), (2005), 869-874.

Electrocatalytic dimerisation of PhBr and PhCH2Br in [BMIM]+NTf2− ionic liquid 
M. Mellah, S.Gmouh, M. Vaultier and V. Jouikov. Electrochem. Comm. 5(7), (2003), 591-593.

Preparation of alternate p-conjugated copolymers involving electrochemically generated aryldizinc intermediates
C. Cecile, M. Mellah, E. Labbé, J.-Y.Nédélec, and J. Périchon. New J. Chem. (2002), 787-790.

Electroreductive polymerisation of 3-substituted 2,5-dihalothiophenes : Direct electrosynthesis vs. stepwise procedure involving thienylzinc intermediates
M. Mellah, E. Labbé, J. Y. Nédélec and J. Périchon, New J. Chem. (2002), 207-212.

New and efficient access to 3-substitued-2,5-dibromothiophenes. Consecutive nickel-catalyzed elctrochemical conversion to thienylzinc species.
M. Mellah, E. Labbé, J. Y. Nédélec and J. Périchon, New J. Chem., 25 (2001), 318-321.

Mukaiyma Aldol and Michael Reactions Catalysed by Lanthanide Iodides
N. Giuseppone, P. Van de Weghe, M. Mellah and J. Collin, Tetrahedron, 54 (1998) 13129-13148