Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Thibaut Duhail"'
Autor:
Jerome Waser, Rosario Scopelliti, Eliott Le Du, Elsa Anselmi, Matthew D. Wodrich, Thibaut Duhail, Emmanuel Magnier, Farzaneh Fadaei-Tirani
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, In press, ⟨10.1002/chem.202101475⟩
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, In press, ⟨10.1002/chem.202101475⟩
Ethynylbenziodoxol(on)e (EBX) cyclic hypervalent iodine reagents have become popular reagents for the alkynylation of radicals and nucleophiles, but only offer limited possibilities for further structure and reactivity fine‐tuning. Herein, the synt
Autor:
Thibaut Duhail, Mingxiang Zhu, Coralie Rombault, Guillaume Dagousset, Samir Messaoudi, Emmanuel Magnier, Elsa Anselmi
Publikováno v:
European Journal of Organic Chemistry. 2022
Autor:
Elsa Anselmi, Antonio Togni, Luca Dell'Amico, Benson J. Jelier, Emmanuel Magnier, Javier Mateos, Guillaume Dagousset, Thibaut Duhail, Tommaso Bortolato
The first light-driven method for the alpha-trifluoromethoxylation of ketones is reported. Enol carbonates, in particular Boc derivatives, react with N-trifluoromethoxy-4-cyano-pyridinium triflimide (2a) using the photoredox-catalyst 4-CzIPN (5 mol-%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce15d7f995b8fc5bde11bde4bb0d93bd
https://doi.org/10.33774/chemrxiv-2021-w1p6g
https://doi.org/10.33774/chemrxiv-2021-w1p6g
Autor:
Emmanuel Magnier, Elsa Anselmi, Tommaso Bortolato, Thibaut Duhail, Luca Dell'Amico, Benson J. Jelier, Guillaume Dagousset, Javier Mateos, Antonio Togni
Publikováno v:
Organic Letters, 23 (18)
Organic Letters
Organic Letters, American Chemical Society, 2021, 23 (18), pp.7088-7093. ⟨10.1021/acs.orglett.1c02494⟩
Organic Letters
Organic Letters, American Chemical Society, 2021, 23 (18), pp.7088-7093. ⟨10.1021/acs.orglett.1c02494⟩
The first light-driven method for the α-trifluoromethoxylation of ketones is reported. Enol carbonates react with N-trifluoromethoxy-4-cyano-pyridinium, using the photoredox catalyst 4-CzIPN under 456 nm irradiation, affording the α-trifluoromethox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15d49f47405378c5a98d91f1e258ebc7
Autor:
Antonio Togni, Nicolas Vanthuyne, Thanh-Nghi Le, Jorna Kalim, Thibaut Duhail, Elsa Anselmi, Emmanuel Magnier
Publikováno v:
Chemical Science, 10 (45)
Chemical Science
Chemical Science, The Royal Society of Chemistry, 2019, 10 (45), pp.10516-10523. ⟨10.1039/c9sc04289j⟩
Chemical Science, 2019, 10 (45), pp.10516-10523. ⟨10.1039/c9sc04289j⟩
Chemical Science
Chemical Science, The Royal Society of Chemistry, 2019, 10 (45), pp.10516-10523. ⟨10.1039/c9sc04289j⟩
Chemical Science, 2019, 10 (45), pp.10516-10523. ⟨10.1039/c9sc04289j⟩
Electrophilic trifluoromethylation is at the forefront of methodologies available for the installation of the CF3 moiety to organic molecules; research in this field is largely spurred by the availability of stable and accessible trifluoromethylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17d96eacb72085ad6ec7a376258bafbc