Georges Fremy
Centre national de la recherche scientifique
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Featured researches published by Georges Fremy.
Tetrahedron Letters | 1995
Eric Monflier; Sébastien Tilloy; Georges Fremy; Yves Castanet; André Mortreux
Abstract Solvent free biphasic hydroformylalion of various water-insoluble terminal olefins can be achieved in high yields and sclcctivitics by using a water-soluble rhodium/triphenylphosphine trisulfonate catalyst and per(2,6-di-o-mclhyl)-β-cyclodcxtrin as inverse phase transfer catalyst. The catalytic activities were up to ten times higher than those observed without pcr(2,6-di-o-methyl)-β-cyclodextrin.
Journal of Organometallic Chemistry | 1995
Georges Fremy; Yves Castanet; Ryszard Grzybek; Eric Monflier; André Mortreux; Anna M. Trzeciak; Józef J. Ziółkowski
Abstract Hydroformylation of methylacrylate to α-aldehyde can be achieved in a two-phase system in the presence of two new water-soluble phosphines. High yields and selectivities of α-aldehyde (ca. 80% with a α/β ratio of 1:20) were obtained. Spectroscopic studies have been carried out and some new rhodium complexes formed in situ in catalytic systems have been identified.
Journal of Molecular Catalysis A-chemical | 1998
Georges Fremy; Eric Monflier; Jean-François Carpentier; Yves Castanet; André Mortreux
Abstract The hydroformylation of various acrylic esters in a two-phase system using a water soluble rhodium complex of trisulfonated triphenylphosphine as catalyst was investigated. The hydroformylation rates of acrylates relatively soluble in water are surprisingly higher in a biphasic system than those observed in a homogenous single-phase system; rate enhancement by a factor of 2–14 can be reached. The role of water on the enhancement of catalytic activity is discussed.
Tetrahedron Letters | 1995
Eric Monflier; Sébastien Tilloy; Georges Fremy; Yolande Barbaux; André Mortreux
Abstract Oxidation of higher α-olefins (C 8 C 16 ) in a two phase system with multicomponents catalytic system, i.e. PdSO 4 /H 9 PV 6 Mo 6 O 40 /CuSO 4 and per(2,6-di- O -methyl)- β -cyclodextrin) gives the corresponding 2-ketones in high yields (>90 %).
Angewandte Chemie | 1995
Eric Monflier; Georges Fremy; Yves Castanet; André Mortreux
Angewandte Chemie | 1995
Georges Fremy; Eric Monflier; Jean-François Carpentier; Yves Castanet; André Mortreux
Journal of Catalysis | 1996
Georges Fremy; Eric Monflier; Jean-François Carpentier; Yves Castanet; André Mortreux
Angewandte Chemie | 1995
Eric Monflier; Georges Fremy; Yves Castanet; André Mortreux
Angewandte Chemie | 1995
Georges Fremy; Jean-François Carpentier; Yves Castanet; Eric Monflier; André Mortreux
Journal of Catalysis | 2005
Emmanuelle Breysse; François Fajula; Annie Finiels; Georges Fremy; Didier Tichit; Claude Moreau