Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Catherine Goux–Henry"'
Publikováno v:
ARKIVOC, Vol 2002, Iss 5, Pp 102-109 (2002)
Externí odkaz:
https://doaj.org/article/1a7a9dfecbcd4719902f4024e8633ad7
Autor:
Jean-Dominique Paoli, Frank Cogordan, Bruno Andrioletti, Lydia A. Heinrich, Catherine Goux-Henry
Publikováno v:
Progress in Organic Coatings. 162:106536
The stability of coil coatings towards exterior influences is one of their most important properties as it ensures substrate quality. The weatherability of eight melamine crosslinked polyester coatings was studied in accelerated aging in order to sys
Publikováno v:
Bioorganic Chemistry
Bioorganic Chemistry, Elsevier, 2018, 77, pp.215-222. ⟨10.1016/j.bioorg.2018.01.005⟩
Bioorganic Chemistry, Elsevier, 2018, 77, pp.215-222. ⟨10.1016/j.bioorg.2018.01.005⟩
Whereas l-3-oxo-hexanoyl homoserine lactone (OHHL) is the active enantiomer of the of LuxR-regulated quorum sensing (QS) autoinducer, its d isomer is implicitly considered as inactive. The present work aims to clarify this l-specificity and investiga
Autor:
Nathalie Kardos, Bruno Andrioletti, François Napoly, Ludivine Jean-Gérard, Micheline Draye, Catherine Goux-Henry
Publikováno v:
Industrial & Engineering Chemistry Research. 54:6046-6051
The hydrogen peroxide mediated oxidative depolymerization of kraft lignin was investigated in the presence of different metal salt catalysts in acetone/water (1/1 v/v) at low temperature. Na2WO4·2H2O appeared to be the best catalyst, yielding four v
Autor:
Eric Framery, Guillaume Pilet, Catherine Goux-Henry, Laurent Copey, Alice D'Onofrio, Ludivine Jean-Gérard, Bruno Andrioletti
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2015, 13 (34), pp.9029-9034
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2015, 13 (34), pp.9029-9034
International audience; D-Glucosamine was successfully employed as a chiral auxiliary for the enantioselective synthesis of phosphine oxides. The influence of the anomeric position was also investigated and revealed the excellent ability of the α-an
Autor:
François Napoly, Micheline Draye, Ludivine Jean-Gérard, Bruno Andrioletti, Catherine Goux-Henry
Publikováno v:
European Journal of Organic Chemistry. 2014:781-787
A novel combination of Fe(TAML)Li and (diacetoxyiodo)benzene for the oxidation of primary and secondary alcohols at 25 °C in acetone is reported. In view of the interesting ability of this system to selectively cleave specific types of C–C bonds o
Autor:
Catherine Goux-Henry, Corine Bas, Nathalie Kardos, Bruno Andrioletti, Laurent Leclerc, Micheline Draye, Gregory Chatel, Emmanuel Naffrechoux
Publikováno v:
Journal of Chemical and Engineering Data
Journal of Chemical and Engineering Data, American Chemical Society, 2012, 57 (12), pp.3385-3390. ⟨10.1021/je300377a⟩
Journal of Chemical and Engineering Data, American Chemical Society, 2012, 57 (12), pp.3385-3390. ⟨10.1021/je300377a⟩
International audience; Energy conversion in sonochemistry is known to be an important factor for understanding the mechanism of chemical reactions. However, ultrasound characteristics are dependent on the physical properties of the liquid medium. Th
Autor:
Mike M. K. Boysen, David Goyard, David Gueyrard, Sébastien Vidal, Susanne M. Telligmann, Eric Framery, Catherine Goux-Henry
Publikováno v:
Tetrahedron Letters. 51:374-377
Two carbohydrate-based spiro bis(isoxazolines) were synthesized via 1,3-dipolar cycloaddition from peracetylated methylene exo-glucal and the corresponding bis(arylnitrile oxide). The bis(cycloadducts) were then evaluated as ligands for enantioselect
Publikováno v:
Tetrahedron: Asymmetry. 18:2782-2786
Chiral fluorous bis(oxazoline)/copper complexes have been applied to the asymmetric glyoxylate-ene reaction, giving moderate to high enantioselectivities. An efficient separation of the copper catalyst using a solid/liquid separation or the FRPSG con
Autor:
Bruno Andrioletti, Ludivine Jean-Gérard, François Napoly, Catherine Goux-Henry, Micheline Draye, Raphaelle Kieffer
Publikováno v:
ChemInform. 46
A new mild and environmental friendly benzylic oxidation with good to excellent yields is presented.