Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Jean-Valère Naubron"'
Autor:
Morgane Mauduit, Stéphane Greff, Gaëtan Herbette, Jean-Valère Naubron, Sara Chentouf, Trung Huy Ngo, Joo-Won Nam, Sacha Molinari, Fathi Mabrouki, Elnur Garayev, Béatrice Baghdikian, Thierry Pérez, Charlotte Simmler
Publikováno v:
ACS Omega, Vol 9, Iss 14, Pp 16877-16878 (2024)
Externí odkaz:
https://doaj.org/article/6ff298d6403c4d3986e239788317c9da
Autor:
Elise Gerometta, Gaëtan Herbette, Elnur Garayev, Arnaud Marvilliers, Jean-Valère Naubron, Carole Di Giorgio, Pierre-Eric Campos, Patricia Clerc, Allison Ledoux, Michel Frederich, Béatrice Baghdikian, Isabelle Grondin, Anne Gauvin-Bialecki
Publikováno v:
Metabolites, Vol 13, Iss 5, p 582 (2023)
Isocaloteysmannic acid (1), a new chromanone, was isolated from the leaf extract of the medicinal species Calophyllum tacamahaca Willd. along with 13 known metabolites belonging to the families of biflavonoids (2), xanthones (3–5, 10), coumarins (6
Externí odkaz:
https://doaj.org/article/efa3948b95e54afcaea675601835da32
Autor:
Jiangkun Ouyang, Anne Swartjes, Marc Geerts, Pieter J. Gilissen, Danni Wang, Paula C. P. Teeuwen, Paul Tinnemans, Nicolas Vanthuyne, Sara Chentouf, Floris P. J. T. Rutjes, Jean-Valère Naubron, Jeanne Crassous, Johannes A. A. W. Elemans, Roeland J. M. Nolte
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
Vibrational circular dichroism (VCD) spectroscopy can be useful for determining the absolute configuration of chiral molecules, as long as the signal intensities are high enough. Here, the authors establish the absolute configurations of two large ch
Externí odkaz:
https://doaj.org/article/0c05c7c5df5042be898233ef4d5a7aa7
Autor:
Georgios Charalambidis, Evangelos Georgilis, Manas K. Panda, Christopher E. Anson, Annie K. Powell, Stephen Doyle, David Moss, Tobias Jochum, Peter N. Horton, Simon J. Coles, Mathieu Linares, David Beljonne, Jean-Valère Naubron, Jonas Conradt, Heinz Kalt, Anna Mitraki, Athanassios G. Coutsolelos, Teodor Silviu Balaban
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)
Artificial light-harvesting systems cannot self-assemble into photon-capturing structures that can reversibly switch into an inactive state. Here, the authors describe a simple and robust dipeptide construct which self-assembles to fibrils, platelets
Externí odkaz:
https://doaj.org/article/d857d55b243b4adeb13a2810eef84c8b
Autor:
Ali Medbouhi, Aura Tintaru, Claire Beaufay, Jean-Valère Naubron, Nassim Djabou, Jean Costa, Joëlle Quetin-Leclercq, Alain Muselli
Publikováno v:
Molecules, Vol 23, Iss 12, p 3250 (2018)
The chemical composition of a hexanic extract of Eryngium campestre, obtained from its aerial parts, was investigated by GC-FID, GC/MS, HRMS, NMR and VCD analyses. The main compounds were germacrene D (23.6%), eudesma-4(15)-7-dien-1-β-ol (8.2%) and
Externí odkaz:
https://doaj.org/article/eec2b9de86d64952ab03b29fb6322642
Autor:
Kévin Masson, Maxime Dousset, Bohdan Biletskyi, Sara Chentouf, Jean‐Valère Naubron, Jean‐Luc Parrain, Laurent Commeiras, Paola Nava, Gaëlle Chouraqui
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, 2023, 365 (7), pp.1002-1011. ⟨10.1002/adsc.202300015⟩
Advanced Synthesis and Catalysis, 2023, 365 (7), pp.1002-1011. ⟨10.1002/adsc.202300015⟩
International audience; An access to functionalised eight-membered carbocyclic ring compounds was developed by simply stirring an unusual vinylogous Donor-Acceptor Cyclopropane (DAC) in boiling o-xylene. Both experimental and computational studies we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::214a99e4fee57a5fbc9d8b297cce5fd5
https://hal.science/hal-04153558
https://hal.science/hal-04153558
Autor:
Danny Wagner, Hagen Kaemmerer, Annie K. Powell, Amer Baniodeh, Nicolas Leblanc, Yan Peng, Stefan Bräse, Christopher E. Anson, Jean-Valère Naubron
Publikováno v:
Chemistry – A European Journal. 27:15103-15109
These 2 coordination clusters are similar but different both in the fine details of their structures as well as their magnetic behaviour. [Fe$_{2}$Dy$_{2}$(μ$_{3}$-OH)$_{2}$(Me-teaH)$_{2}$(O$_{2}$CPh)$_{6}$], which normally forms with the racemic ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fca987ba9a7ab7941fb7e67e11e6f6d8
https://doi.org/10.1002/chem.202103360
https://doi.org/10.1002/chem.202103360
Autor:
Morgane Mauduit, Stéphane Greff, Gaëtan Herbette, Jean-Valère Naubron, Sara Chentouf, Trung Huy Ngo, Joo-Won Nam, Sacha Molinari, Fathi Mabrouki, Elnur Garayev, Béatrice Baghdikian, Thierry Pérez, Charlotte Simmler
Publikováno v:
ACS Omega
ACS Omega, 2022, 7 (47), pp.43068-43083. ⟨10.1021/acsomega.2c05415⟩
ACS Omega, 2022, 7 (47), pp.43068-43083. ⟨10.1021/acsomega.2c05415⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68be5692ff30c47e7de569450cfd1c56
https://hal.science/hal-03857501
https://hal.science/hal-03857501
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, 2022, 61 (50), ⟨10.1002/anie.202214763⟩
Angewandte Chemie International Edition, 2022, 61 (50), ⟨10.1002/anie.202214763⟩
International audience; We report here the development of a rotating molecular switch based on metal-catalyzed reversible (de)-hydrogenation. Under an argon atmosphere, acceptorless dehydrogenation induces a switch from an alcohol to a ketone, while
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a7cb5f156fe0fcbd67a77299368632b
https://doi.org/10.1002/ange.202214763
https://doi.org/10.1002/ange.202214763
Autor:
Guillaume Dauvergne, Jean‐Valère Naubron, Michel Giorgi, Xavier Bugaut, Jean Rodriguez, Yannick Carissan, Yoann Coquerel
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, 2022, pp.e202202473. ⟨10.1002/chem.202202473⟩
Chemistry-A European Journal, 2022, pp.e202202473. ⟨10.1002/chem.202202473⟩
International audience; The synthetic equivalents of the enantiopure binaphthyl bis(aryne) atropisomers derived from BINOL (1,1'bi-2,2'-naphtol) featuring a stereogenic axis vicinal to the two reactive triple bonds can be generated for the first time
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e3e8f7e960f6e033f2ef30e9e893b14
https://doi.org/10.1002/chem.202202473
https://doi.org/10.1002/chem.202202473