Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Héloïse Dossmann"'
Autor:
Fen Zhao, Mehdi Abdellaoui, Wided Hagui, Maria Ballarin-Marion, Jérôme Berthet, Vincent Corcé, Stéphanie Delbaere, Héloïse Dossmann, Agathe Espagne, Jérémy Forté, Ludovic Jullien, Thomas Le Saux, Virginie Mouriès-Mansuy, Cyril Ollivier, Louis Fensterbank
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
Dual photo- and metal-catalysis is generally not well-understood when the metal catalyst is a gold complex. Here the authors show that a variation of a known metallaphotoredox annulation is possible without an added photocatalyst, proceeding putative
Externí odkaz:
https://doaj.org/article/f93f92b3403e41b38c6464d5032429e7
Autor:
Anissa Beghennou, Geoffrey Gontard, Héloïse Dossmann, Kévin Passador, Serge Thorimbert, Vincent Corcé, Candice Botuha
Publikováno v:
Organic & Biomolecular Chemistry. 21:2976-2982
Original fluorescent dyes containing 1,6-naphthyridin-7(6H)-one have been synthesized and their optical properties have been studied.
Autor:
Alexander Mamontov, Liang Chang, Héloïse Dossmann, Benoît Bertrand, Luc Dechoux, Serge Thorimbert
Publikováno v:
Organic letters.
Commercially available Fe(TTP)Cl catalyzes three-component dearomative formal cycloaddition reactions between pyridines, diazo compounds, and coumalates. Diversely substituted annelated seven-membered N-heterocycles could be generated in less than 10
Autor:
Fen Zhao, Mehdi Abdellaoui, Wided Hagui, Maria Ballarin-Marion, Jérôme Berthet, Vincent Corcé, Stéphanie Delbaere, Héloïse Dossmann, Agathe Espagne, Jérémy Forté, Ludovic Jullien, Thomas Le Saux, Virginie Mouriès-Mansuy, Cyril Ollivier, Louis Fensterbank
Publikováno v:
Nature Communications
Nature Communications, 2022, 13 (1), pp.2295. ⟨10.1038/s41467-022-29982-2⟩
Nature Communications, 2022, 13, pp.470. ⟨10.1038/s41467-022-29982-2⟩
Nature Communications, 2022, 13 (1), pp.2295. ⟨10.1038/s41467-022-29982-2⟩
Nature Communications, 2022, 13, pp.470. ⟨10.1038/s41467-022-29982-2⟩
Photosensitization of organogold intermediates is an emerging field in catalysis. In this context, an access to 2,3-disubstituted indoles from o-alkynyl aniline and iodoalkyne derivatives via a gold-catalyzed sequence under visible-light irradiation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5edbc6ffb43c28248878cada0dc81e40
https://hal.science/hal-03813241/file/s41467-022-29982-2.pdf
https://hal.science/hal-03813241/file/s41467-022-29982-2.pdf
Publikováno v:
Chemistry – A European Journal. 26:12846-12861
The two independent and NN^ coordination sites of a newly synthesized bis[2-(hydroxyphenyl)-1,2,4-triazole] platform have been exploited to prepare four monometallic neutral ()PtII complexes carrying DMSO, pyridine, triphenylphosphine, or N-heterocyc
Autor:
Fen, Zhao, Mehdi, Abdellaoui, Wided, Hagui, Maria, Ballarin-Marion, Jérôme, Berthet, Vincent, Corcé, Stéphanie, Delbaere, Héloïse, Dossmann, Agathe, Espagne, Jérémy, Forté, Ludovic, Jullien, Thomas, Le Saux, Virginie, Mouriès-Mansuy, Cyril, Ollivier, Louis, Fensterbank
Publikováno v:
Nature communications. 13(1)
Photosensitization of organogold intermediates is an emerging field in catalysis. In this context, an access to 2,3-disubstituted indoles from o-alkynyl aniline and iodoalkyne derivatives via a gold-catalyzed sequence under visible-light irradiation
Autor:
Vincent Corcé, Jérôme Berthet, Mehdi Abdellaoui, Héloïse Dossmann, Louis Fensterbank, Fen Zhao, Cyril Ollivier, Virginie Mouriès-Mansuy, Stéphanie Delbaere, Thomas Le Saux, Jérémy Forté, Ludovic Jullein, Agathe Espagne
A novel access to 2,3-disubstituted indoles from o-alkynyl aniline and iodoalkyne derivatives via a gold-catalyzed sequence under visible-light irradiation and in the absence of an exogenous photocatalyst was uncovered. A wide scope of the process wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::437ae88b8f959e60ac042957d28b9478
https://doi.org/10.26434/chemrxiv-2021-vfvkd
https://doi.org/10.26434/chemrxiv-2021-vfvkd
Autor:
Silva, Khodjoyan, Edwyn, Remadna, Héloïse, Dossmann, Denis, Lesage, Geoffrey, Gontard, Jérémy, Forté, Henrik, Hoffmeister, Uttara, Basu, Ingo, Ott, Philip, Spence, Zoë A E, Waller, Michèle, Salmain, Benoît, Bertrand
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 27(63)
A library of eleven cationic gold(III) complexes of the general formula [(C C)Au(N N)]
Autor:
Cédric Przybylski, Anne Ponchel, Teddy Weisgerber, Lucas Fontaine, Véronique Bonnet, Héloïse Dossmann, Eric Monflier
Publikováno v:
Inorganic Chemistry
Inorganic Chemistry, American Chemical Society, 2021, 60 (2), pp.930-943. ⟨10.1021/acs.inorgchem.0c03052⟩
Inorganic Chemistry, 2021, 60 (2), pp.930-943. ⟨10.1021/acs.inorgchem.0c03052⟩
Inorganic Chemistry, American Chemical Society, 2021, 60 (2), pp.930-943. ⟨10.1021/acs.inorgchem.0c03052⟩
Inorganic Chemistry, 2021, 60 (2), pp.930-943. ⟨10.1021/acs.inorgchem.0c03052⟩
International audience; Cyclodextrins (CDs) are cyclic oligosaccharides mainly composed of six, seven, and eight glucose units, so-called α-, β-, and γ-CDs, respectively. They own a very particular molecular structure exhibiting hydrophilic featur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08f659598c9bd003705d58b8cd2f14e7
https://hal.archives-ouvertes.fr/hal-03116156
https://hal.archives-ouvertes.fr/hal-03116156
Autor:
Geoffrey Gontard, Michèle Salmain, Uttara Basu, Philip Spence, Denis Lesage, Jérémy Forté, Henrik Hoffmeister, Edwyn Remadna, Silva Khodjoyan, Benoît Bertrand, Héloïse Dossmann, Ingo Ott, Zoë A. E. Waller
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, In press, ⟨10.1002/chem.202102751⟩
Chemistry-A European Journal, Wiley-VCH Verlag, In press, ⟨10.1002/chem.202102751⟩
International audience; A library of eleven cationic gold(III) complexes of the general formula [(C^C)Au(N^N)] + when C^C is either biphenyl or 4,4’-ditertbutyldiphenyl and N^N is a bipyridine, phenanthroline or dipyridylamine derivative have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc14a215258dc4bf0964e09386aa2b46
https://hal.archives-ouvertes.fr/hal-03351025/document
https://hal.archives-ouvertes.fr/hal-03351025/document