Dr. Nicolas VANTHUYNE
Dr.
Nicolas
VANTHUYNE
AMU iSm2 Service 432
Campus Scientifique de St Jérôme
13397
Marseille cedex 20
Téléphone :
Courriel :
Parcours :
2004 Doctorat de chimie organique (Université “Paul Cézanne”, Aix-Marseille III)
2000 Ingénieur ENSSPICAM (Ecole Nationale Supérieure de Synthèses, de Procédés et d'Ingénierie d'Aix-Marseille) et Diplôme d’Etudes Approfondies de Chimie et Physico-Chimie Moléculaire Organique (Université “Paul Cézanne”, Aix-Marseille III)
Thématiques :
Séparations analytiques et préparatives d’énantiomères par chromatographie liquide chirale
Stéréochimie dynamique
Publications (245)
Reference
Résumé graphique
HAL
Geometric enantiomerism in cyclic compounds: Chiral dibrominated 1,3-dioxanes
Crina Cismaş, Nicolas Vanthuyne, Hélène Rispaud, Richard Attila Varga, Elena Bogdan, Christian Roussel, Ion Grosu, Chirality, 2011, 23, 167-171. <hal-02517509>
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Inherently chiral phosphonatocavitands as artificial chemo- and enantio-selective receptors of natural ammoniums
Jérôme Vachon, Steven Harthong, Erwann Jeanneau, Christophe Aronica, Nicolas Vanthuyne, Christian Roussel, Jean-Pierre Dutasta, Organic and Biomolecular Chemistry, 2011, 9, 5086-5091. <hal-01116903>
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An efficient and recyclable hybrid nanocatalyst to promote enantioselective radical cascade rearrangements of enediynes
Malek Nechab, Eric Besson, Damien Campolo, Patricia Perfetti, Nicolas Vanthuyne, Emily Bloch, Renaud Denoyel, Michèle P. Bertrand, Chemical Communications, 2011, 47, 5286--5288. <hal-01460335>
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Hemisynthesis and Odour Properties of ?-hydroxy-?-lactones and precursors derived from linalool.
F. MEHL, I. BOMBARDA, N. VANTHUYNE, R. FAURE, E.M. GAYDOU. Food Chemistry, 2010, 121(1), 98-104.
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Ridge-tile-like chiral topology: Synthesis, resolution, and complete chiroptical characterization of enantiomers of edge-sharing binuclear square planar complexes of Ni(II) bearing achiral ligands
V. Soloshonok, T. Ono, H. Ueki, N. Vanthuyne, T. S. Balaban, J. Bürck, H. Fliegl, W. Klopper, J.-V. Naubron, T. T. T. Bui, A. F. Drake and C. Roussel, J. Am. Chem. Soc. 2010, 132, 10477-10483.-
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Memory of Chirality in Cascade Rearrangements of Enediynes
Malek Nechab, Damien Campolo, Julien Maury, Patricia Perfetti, Nicolas Vanthuyne, Didier Siri, Michèle P. Bertrand, Journal of the American Chemical Society, 2010, 132, 14742--14744. <hal-01460245>
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Chiral oxorhenium(V) complexes as candidates for the experimental observation of molecular parity violation: a structural, synthetic and theoretical study.
Frederic de Montigny, Radovan Bast, Andre Severo Pereira Gomes, Guillaume Pilet, Nicolas Vanthuyne, Christian Roussel, Laure Guy, Peter Schwerdtfeger, Trond Saue, Jeanne Crassous, Physical Chemistry Chemical Physics, 2010, 12, 8792-803. <hal-00760991>
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Persistent mixed-valence [(TTF)2]+* dyad of a chiral bis(binaphthol)-tetrathiafulvalene (TTF) derivative.
Ali Saad, Frédéric Barrière, Eric Levillain, Nicolas Vanthuyne, Olivier Jeannin, Marc Fourmigué, Chemistry - A European Journal, 2010, 16, 8020-8. <hal-00502155>
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The absolute configuration of an inherently chiral phosphonatocavitand and its use toward the enantioselective recognition of l-adrenaline
Jérôme Vachon, Steven Harthong, Béatrice Dubessy, Jean-Pierre Dutasta, Nicolas Vanthuyne, Christian Roussel, Jean-Valère Naubron, Tetrahedron: Asymmetry, 2010, 21, 1534–1541. <hal-01116894>
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Chiral separation of hesperidin and naringin and its analysis in a butanol extract of Launeae arborescens
Nasser Belboukhari, Abdelkrim Cheriti, Christian Roussel, Nicolas Vanthuyne, Natural Product Research, 2010, 24, 669-681. <hal-02517480>
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Pages
Communications orales et par affiche (3)
Reference
Résumé graphique
HAL
Kais Dhbaibi, Monika Srebro-Hooper, Philippe Blanchard, Clément Cabanetos, Nicolas Vanthuyne, et al.. Design d’émetteurs hélicèniques pour l’élaboration d’OLEDs chirales. Science et Technologie des systèmes Pi-Conjugués (SPIC), Oct 2019, Arras, France. ⟨hal-02922011⟩
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Cécile Mézière, Magali Allain, Cristina Oliveras-Gonzalez, Thomas Cauchy, Nicolas Vanthuyne, et al.. Tetrathiafulvalene-[2.2]paracyclophanes: Synthesis, chiral structures and chiroptical properties. Journées André Collet de la Chiralité, 2018, Noirmoutier, France. 2018. ⟨hal-02564566⟩
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Ludovic Favereau, Monika Srebro-Hooper, Francesco Zinna, Philippe Blanchard, Clément Cabanetos, et al.. Matériaux moléculaires chiraux pour l'optoélectronique. SPIC 2017, Oct 2017, Limoges, France. ⟨hal-02888985⟩
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Chapitres d'ouvrages (2)
Reference
Résumé graphique
HAL
Nicolas Vanthuyne, Christian Roussel. Chiroptical Detectors for the Study of Unusual Phenomena in Chiral Chromatography. Topics in Current Chemistry, Differentiation of Enantiomers I, pp.107-151, 2013, ⟨10.1007/128_2013_441⟩. ⟨hal-02528021⟩
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Ibon Alkorta, José Elguero, Christian Roussel, Nicolas Vanthuyne, Patrick Piras. Atropisomerism and Axial Chirality in Heteroaromatic Compounds. Advances in Heterocyclic Chemistry, 105, pp.1-188, 2012, ⟨10.1016/B978-0-12-396530-1.00001-2⟩. ⟨hal-02517553⟩
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2004 Doctorat de chimie organique (Université “Paul Cézanne”, Aix-Marseille III)
2000 Ingénieur ENSSPICAM (Ecole Nationale Supérieure de Synthèses, de Procédés et d'Ingénierie d'Aix-Marseille) et Diplôme d’Etudes Approfondies de Chimie et Physico-Chimie Moléculaire Organique (Université “Paul Cézanne”, Aix-Marseille III)
Séparations analytiques et préparatives d’énantiomères par chromatographie liquide chirale
Stéréochimie dynamique
Reference | Résumé graphique | HAL |
---|---|---|
Geometric enantiomerism in cyclic compounds: Chiral dibrominated 1,3-dioxanes |
![]() |
✓ |
Inherently chiral phosphonatocavitands as artificial chemo- and enantio-selective receptors of natural ammoniums |
![]() |
✖ |
An efficient and recyclable hybrid nanocatalyst to promote enantioselective radical cascade rearrangements of enediynes |
![]() |
✖ |
Hemisynthesis and Odour Properties of ?-hydroxy-?-lactones and precursors derived from linalool. |
![]() |
✖ |
Ridge-tile-like chiral topology: Synthesis, resolution, and complete chiroptical characterization of enantiomers of edge-sharing binuclear square planar complexes of Ni(II) bearing achiral ligands |
![]() |
✖ |
Memory of Chirality in Cascade Rearrangements of Enediynes |
![]() |
✖ |
Chiral oxorhenium(V) complexes as candidates for the experimental observation of molecular parity violation: a structural, synthetic and theoretical study. |
![]() |
✓ |
Persistent mixed-valence [(TTF)2]+* dyad of a chiral bis(binaphthol)-tetrathiafulvalene (TTF) derivative. |
![]() |
✓ |
The absolute configuration of an inherently chiral phosphonatocavitand and its use toward the enantioselective recognition of l-adrenaline |
![]() |
✖ |
Chiral separation of hesperidin and naringin and its analysis in a butanol extract of Launeae arborescens |
![]() |
✖ |
Pages
Reference | Résumé graphique | HAL |
---|---|---|
Kais Dhbaibi, Monika Srebro-Hooper, Philippe Blanchard, Clément Cabanetos, Nicolas Vanthuyne, et al.. Design d’émetteurs hélicèniques pour l’élaboration d’OLEDs chirales. Science et Technologie des systèmes Pi-Conjugués (SPIC), Oct 2019, Arras, France. ⟨hal-02922011⟩ |
![]() |
✖ |
Cécile Mézière, Magali Allain, Cristina Oliveras-Gonzalez, Thomas Cauchy, Nicolas Vanthuyne, et al.. Tetrathiafulvalene-[2.2]paracyclophanes: Synthesis, chiral structures and chiroptical properties. Journées André Collet de la Chiralité, 2018, Noirmoutier, France. 2018. ⟨hal-02564566⟩ |
![]() |
✓ |
Ludovic Favereau, Monika Srebro-Hooper, Francesco Zinna, Philippe Blanchard, Clément Cabanetos, et al.. Matériaux moléculaires chiraux pour l'optoélectronique. SPIC 2017, Oct 2017, Limoges, France. ⟨hal-02888985⟩ |
![]() |
✖ |
Reference | Résumé graphique | HAL |
---|---|---|
Nicolas Vanthuyne, Christian Roussel. Chiroptical Detectors for the Study of Unusual Phenomena in Chiral Chromatography. Topics in Current Chemistry, Differentiation of Enantiomers I, pp.107-151, 2013, ⟨10.1007/128_2013_441⟩. ⟨hal-02528021⟩ |
![]() |
✓ |
Ibon Alkorta, José Elguero, Christian Roussel, Nicolas Vanthuyne, Patrick Piras. Atropisomerism and Axial Chirality in Heteroaromatic Compounds. Advances in Heterocyclic Chemistry, 105, pp.1-188, 2012, ⟨10.1016/B978-0-12-396530-1.00001-2⟩. ⟨hal-02517553⟩ |
![]() |
✖ |