Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Sébastien Redon"'
Autor:
Oscar Leonardo Avendaño Leon, Christophe Curti, Hussein El-Kashef, Youssef Kabri, Sébastien Redon, Patrice Vanelle
Publikováno v:
Molbank, Vol 2023, Iss 4, p M1750 (2023)
As part of our ongoing attempt to broaden the applications of the amidoxime moiety as a potential source of new antileishmanial agents, this study focuses on the product 4-(5-Benzyl-3-((4-fluorophenyl)sulfonyl)-5-methyl-4,5-dihydrofuran-2-yl)-2-nitro
Externí odkaz:
https://doaj.org/article/3a74bde867f145cfab83e73775a31ebd
Autor:
Oscar Leonardo Avendaño Leon, Christophe Curti, Fabiana Maia Santos Urbancg Moncorvo, Youssef Kabri, Sébastien Redon, Eduardo Caio Torres-Santos, Romain Paoli-Lombardo, Patrice Vanelle
Publikováno v:
Molbank, Vol 2023, Iss 4, p M1736 (2023)
As part of our ongoing research into the antileishmanial properties of amidoxime derivatives, we report a preliminary assessment of the antiparasitic properties of a novel compound, diethyl (5-benzyl-2-(4-(N′-hydroxycarbamimidoyl)phenyl)-5-methyl-4
Externí odkaz:
https://doaj.org/article/e55fadfa457e490a80ac0f4274d10c39
Publikováno v:
Synlett.
An unprecedented I2/sulfinate thiolating system is described for the sulfenylation of electron-rich heterocycles. This phosphine-free strategy permits simple, efficient, and fast sulfenylation of imidazo heterocycles, anilines, indoles, coumarins, or
Autor:
Arona Fall, Guillaume Tintori, David Bergé-Lefranc, Yuxi Zhao, Patrice Vanelle, Nadhrata Assani, Sébastien Redon, Julie Broggi
Publikováno v:
Organic Chemistry Frontiers
Organic Chemistry Frontiers, 2021, 8 (6), pp.1197-1205. ⟨10.1039/d0qo01488e⟩
Organic Chemistry Frontiers, Royal Society of Chemistry, 2021, 8 (6), pp.1197-1205. ⟨10.1039/d0qo01488e⟩
Organic Chemistry Frontiers, 2021, 8 (6), pp.1197-1205. ⟨10.1039/d0qo01488e⟩
Organic Chemistry Frontiers, Royal Society of Chemistry, 2021, 8 (6), pp.1197-1205. ⟨10.1039/d0qo01488e⟩
International audience; Organic electron donors (OEDs) are increasingly used as efficient reducing agents in various radical reactions. However, their sensitivity to air restraints their practical use and the development of further industrial applica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67e7dcfce1009fdd8391eeba89083afb
https://hal.science/hal-03142833
https://hal.science/hal-03142833
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2020, 85 (5), pp.3071-3081. ⟨10.1021/acs.joc.9b02963⟩
Journal of Organic Chemistry, 2020, 85 (5), pp.3071-3081. ⟨10.1021/acs.joc.9b02963⟩
Journal of Organic Chemistry, American Chemical Society, 2020, 85 (5), pp.3071-3081. ⟨10.1021/acs.joc.9b02963⟩
Journal of Organic Chemistry, 2020, 85 (5), pp.3071-3081. ⟨10.1021/acs.joc.9b02963⟩
The dichalcogenation of imidazoheterocycles led to the first functionalization of imidazo[1,2-a]pyrimidine cores on the C6-position. The methodology, involving iodine/dimethylsulfoxide oxidation of diaryldichalcogenides, started with C3-chalcogenatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ca5575212908bfabe977ac39622e785
https://hal-amu.archives-ouvertes.fr/hal-02560703
https://hal-amu.archives-ouvertes.fr/hal-02560703
Autor:
Martin Ipuy, Erwann Jeanneau, Sébastien Redon, Alain Ibanez, Chantal Andraud, Gwenaelle Eucat, Yann Bretonnière, Isabelle Gautier-Luneau
Publikováno v:
Dyes and Pigments
Dyes and Pigments, 2018, 156, pp.116-132. ⟨10.1016/j.dyepig.2018.03.049⟩
Dyes and Pigments, Elsevier, 2018, 156, pp.116-132. ⟨10.1016/j.dyepig.2018.03.049⟩
Dyes and Pigments, 2018, 156, pp.116-132. ⟨10.1016/j.dyepig.2018.03.049⟩
Dyes and Pigments, Elsevier, 2018, 156, pp.116-132. ⟨10.1016/j.dyepig.2018.03.049⟩
International audience; Series of solid-state emitters based on the D-π-A dipolar structure and featuring various electron-donor and electron-acceptor groups were designed, and their spectroscopic properties studied. From weak emission in dilute sol
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2018, 29 (09), pp.1215-1218. ⟨10.1055/s-0037-1609340⟩
SYNLETT, 2018, 29 (09), pp.1215-1218. ⟨10.1055/s-0037-1609340⟩
SYNLETT, Georg Thieme Verlag, 2018, 29 (09), pp.1215-1218. ⟨10.1055/s-0037-1609340⟩
SYNLETT, 2018, 29 (09), pp.1215-1218. ⟨10.1055/s-0037-1609340⟩
International audience; A sequential one pot, simple and convenient method is described for the synthesis of 3-selenocyanato-4H-chromen-4-ones by addition first of DMF-DMA then of triselenodicyanide as electrophile.
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2019, 51 (19), pp.3758-3764. ⟨10.1055/s-0039-1690013⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2019, 51 (19), pp.3758-3764. ⟨10.1055/s-0039-1690013⟩
SYNTHESIS, Georg Thieme Verlag, 2019, 51 (19), pp.3758-3764. ⟨10.1055/s-0039-1690013⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2019, 51 (19), pp.3758-3764. ⟨10.1055/s-0039-1690013⟩
International audience; The first ipso-selenocyanation of arylboronic acids is achieved using selenium dioxide and malononitrile under mild conditions. The reaction is successful even without metal or base in DMSO. The major advantages of this new me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64fb42989d51c796489252f025bb6d85
https://hal.archives-ouvertes.fr/hal-02319333
https://hal.archives-ouvertes.fr/hal-02319333
Autor:
Maxime Rémond, Chantal Andraud, Zheng Zheng, Yann Bretonnière, Sébastien Redon, Erwann Jeanneau
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, 2019, 84 (16), pp.9965-9974. ⟨10.1021/acs.joc.9b01120⟩
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (16), pp.9965-9974. ⟨10.1021/acs.joc.9b01120⟩
Journal of Organic Chemistry, 2019, 84 (16), pp.9965-9974. ⟨10.1021/acs.joc.9b01120⟩
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (16), pp.9965-9974. ⟨10.1021/acs.joc.9b01120⟩
International audience; In the context of molecular engineering of push−pull dipolar dyes, we introduce a structural modification of the well-known electron-accepting group 2-dicyanomethylidene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran (TCF). Introd
Autor:
Yulia A. Getmanenko, Yann Bretonnière, Simon Pascal, Iryna Davydenko, Isabelle Ledoux-Rak, Stephen Barlow, Chantal Andraud, Minh Ngo, Yadong Zhang, Seth R. Marder, Guillaume Pilet, Sébastien Redon, Olivier Maury
Publikováno v:
Chemistry of Materials
Chemistry of Materials, 2018, 30 (10), pp.3410-3418. ⟨10.1021/acs.chemmater.8b00960⟩
Chemistry of Materials, American Chemical Society, 2018, 30 (10), pp.3410-3418. ⟨10.1021/acs.chemmater.8b00960⟩
Chemistry of Materials, 2018, 30 (10), pp.3410-3418. ⟨10.1021/acs.chemmater.8b00960⟩
Chemistry of Materials, American Chemical Society, 2018, 30 (10), pp.3410-3418. ⟨10.1021/acs.chemmater.8b00960⟩
International audience; Fifteen heptamethine dyes in which a tricyanofuran acceptor is linked to donors of different strength were synthesized, and their absorption, thermal, electrochemical, and second-order nonlinear optical properties were investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff8f67cec5045965dc09fab70e16375c
https://hal.science/hal-01957768/document
https://hal.science/hal-01957768/document