Marcel Lefort
Rhône-Poulenc
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Featured researches published by Marcel Lefort.
Tetrahedron Letters | 1980
Marcel Lefort; Christian Simmonet; Marc Birot; Gérard Déléris; J. Dunogues; Raymond Calas
Abstract Allyltrichlorosilanes are prepared according to a one-step regiospecific process based on the reaction of allyl chlorides with SiCl 4 and NiCp 2 /HMPA (catalyst), in the presence of industrial methylchlorodisilane fraction. 4 Benzyltrihalosilanes are similarly obtained.
Journal of Organometallic Chemistry | 1984
Gérard Déléris; Marc Birot; J. Dunogues; Bernard Barbe; Michel Petraud; Marcel Lefort
Abstract The selective population transfer (SPT) technique has been applied to 29 Si NMR of the complete series of methylchlorodisilylmethanes, several of which are new compounds. A great enhancement of the signals was observed and unambiguous assignments based on the determination of 2 J (SiH) coupling constants could be made. The first example of this type is presented.
Journal of Organometallic Chemistry | 1978
Raymond Calas; Gérard Déléris; J. Dunogues; Marcel Lefort; Christian Simmonet
Abstract The chlorodisilane residue from the industrial synthesis of methylchlorosilanes is cleaved under hydrogen (25 bars) in the presence of HMPT/nickelocene mixture or nickel (resulting from the reduction of dry NiCl 2 by Et 3 SiH) and leads to the formation of methyldichlorosilane (noble product), to the detriment of the methyltrichlorosilane (much less noble). This reaction also gives an appreciable amount of the rare and very useful dimethylchlorosilane.
Synthetic Communications | 1984
Jean-Paul Picard; J. Dunogues; Abdelaziz Elyusufi; Marcel Lefort
Abstract The use of a nickel catalyst (“Ni/SiH”) allows easy hydrogenation of alkenylchlorosilanes at atmospheric pressure, not affecting the chlorine function, and leads to quantitative synthesis of alkylchlorosilanes.
Journal of Organometallic Chemistry | 1981
Gerard Simon; Marcel Lefort; Marc Birot; J. Dunogues; N. Duffaut; R. Calas
Abstract Partial reduction of MeSiCl 3 and Me 2 SiCl 2 using CaH 2 or (TiH 2 ) n at high temperature (300°C) leads to MeSiHCl 2 and Me 2 SiHCl, respectively, in good yields but in low proportion. In the presence of AlCl 3 as catalyst the reaction affords Me 2 SiCl 2 and Me 3 SiCl, in yields higher than those previously observed in the absence of a reducing agent. These redistribution reactions involve MeSiHCl 2 and Me 2 SiHCl as intermediates. Consequently Me 2 SiHCl with or without Me 2 SiCl 2 and Alcl 3 deposited on carbon black as catalyst can undergo disproportionation to give Me 3 SiCl.
Archive | 1978
Michel Bargain; Marcel Lefort
Archive | 1977
Raymond Calas; J. Dunogues; Gerard Deleris; Marcel Lefort; Christian Simonnet
Archive | 1975
Gilbert Marin; Marcel Lefort
Archive | 1968
Louis Ceyzeriat; Maurice Henri Robert J Gaignon; Marcel Lefort
Archive | 1977
Michel Bargain; Marcel Lefort