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Marc Lemaire

Researcher at Claude Bernard University Lyon 1

Publications -  403
Citations -  9863

Marc Lemaire is an academic researcher from Claude Bernard University Lyon 1. The author has contributed to research in topics: Catalysis & Enantioselective synthesis. The author has an hindex of 48, co-authored 399 publications receiving 9317 citations. Previous affiliations of Marc Lemaire include Centre national de la recherche scientifique & Blaise Pascal University.

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Nitrogen-containing ligands for asymmetric homogeneous and heterogeneous catalysis.

TL;DR: It is shown here how the structure of the C−O Bond Formation following C−H Bond Oxidation following Baeyer−Villiger-type Reaction and Wacker-type Cyclization influenced the formation of the S−N Bond Formation.
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Alkyldibenzothiophenes Hydrodesulfurization-Promoter Effect, Reactivity, and Reaction Mechanism

TL;DR: In this article, the effect of Co or Ni on the HDS activity of Mo/alumina was studied by using dibenzothiophene (DBT) and 4,6-dimethyldibenzethiophene(46DMDBT), and the reaction was carried out at 340°C under a 4 MPa total pressure.
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Deep desulfurization: reactions, catalysts and technological challenges

TL;DR: The design of future processes is based on the identification of the refractory sulfur compounds and the knowledge of their individual reactivity and in the presence of inhibitors, as illustrated in this paper.
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Effects of steric factors on the electrosynthesis and properties of conducting poly(3-alkylthiophenes)

TL;DR: In this paper, a series of thiophene monomers 3-substituted with linear and branched alkyl chains have been synthesized, and their electropolymerization has been investigated together with the properties of the resulting polymers.
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Poly mono-, bi- and trithiophene: effect of oligomer chain length on the polymer properties

TL;DR: In this article, a comparison of the electrical, electrochemical and spectroscopic properties of the resulting polymers reveals a steady decrease of their conjugation length as the chain length of the starting oligomer increases.