Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Killian Onida"'
Publikováno v:
Green Chemistry.
The chemical upcycling of poly(bisphenol A carbonate) was carried out through organocatalysis using α-hydroxyketones as nucleophiles, leading to valuable vinylene carbonates.
Autor:
Christophe Boisson, Killian Onida, Sébastien Norsic, Alice J. Haddleton, Franck D'Agosto, Nicolas Duguet
Publikováno v:
Advanced Synthesis & Catalysis. 363:5129-5137
Autor:
Adeline Lavoignat, Nicolas Duguet, Thomas De Dios Miguel, Stéphane Picot, Killian Onida, Dan Louvel
Publikováno v:
Synthesis. 54:617-628
The peracetalization of a β-hydroxy hydroperoxide derived from methyl oleate was studied using benzaldehyde as a model substrate to give the corresponding fatty 1,2,4-trioxane. The desired product was obtained as a mixture of regioisomers but only o
Publikováno v:
European Journal of Organic Chemistry. 2022
Substituted vinylene carbonates were directly prepared from aromatic aldehydes following a one-pot Benzoin condensation / transcarbonation sequence under solvent-free conditions. The combination of a N-phenyl substituted triazolium salt NHC precursor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2a873d4ffb7da0fb44486ba0affd404
https://doi.org/10.26434/chemrxiv-2021-mw0p5
https://doi.org/10.26434/chemrxiv-2021-mw0p5
Autor:
Killian Onida, Alice J. Haddleton, Sébastien Norsic, Christophe Boisson, Franck D'Agosto, Nicolas Duguet
The organocatalytic synthesis of vinylene carbonates from benzoins and acyloins was studied using diphenyl carbonate as a carbonyl source. A range of N-Heterocyclic Carbene (NHC) precursors were screened and it was found that imidazolium salts were t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecd61404807294cb119348bfa48c3456
https://doi.org/10.26434/chemrxiv-2021-mm08f
https://doi.org/10.26434/chemrxiv-2021-mm08f
Autor:
Sébastien Norsic, Killian Onida, Christophe Boisson, Franck D'Agosto, Nicolas Duguet, Alice J. Haddleton
The organocatalytic synthesis of vinylene carbonates from benzoins and acyloins was studied using diphenyl carbonate as a carbonyl source. A range of N-Heterocyclic Carbene (NHC) precursors were screened and it was found that imidazolium salts were t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca9164f7ae5bc8d4f2e0b11e2681550
https://doi.org/10.33774/chemrxiv-2021-mm08f
https://doi.org/10.33774/chemrxiv-2021-mm08f
Publikováno v:
European Journal of Organic Chemistry. 2019:6106-6109
Thermomorphic Polyethylene‐Supported Organocatalysts for the Valorization of Vegetable Oils and CO 2
Autor:
Sébastien Norsic, Killian Onida, Nam Duc Vu, Ayman Akhdar, Franck D'Agosto, Nicolas Duguet, Christophe Boisson, Kevin Grollier
Publikováno v:
Advanced Sustainable Systems
Advanced Sustainable Systems, Wiley, 2021, 5 (2), pp.2000218. ⟨10.1002/adsu.202000218⟩
Advanced Sustainable Systems, Wiley, 2021, 5 (2), pp.2000218. ⟨10.1002/adsu.202000218⟩
International audience; A range of thermomorphic polyethylene-supported organocatalysts is prepared from N-alkyl imidazoles and polyethylene iodide (PE) with good yields (85–92%) and high funtionality (98–99%). The catalytic activity of these spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a08e036628fbfb39b9e0a4c7d9fcef1a
https://hal.archives-ouvertes.fr/hal-03245780/document
https://hal.archives-ouvertes.fr/hal-03245780/document
Autor:
Antonio Reina, Didier Bouyssi, Erwann Jeanneau, Killian Onida, Nuno Monteiro, Abderrahmane Amgoune, Tetiana Krachko
Publikováno v:
ACS Catalysis
ACS Catalysis, American Chemical Society, 2020, 10 (3), pp.2189-2197. ⟨10.1021/acscatal.9b05159⟩
ACS Catalysis, American Chemical Society, 2020, 10 (3), pp.2189-2197. ⟨10.1021/acscatal.9b05159⟩
This study describes the development and understanding of a palladium-catalyzed cross-coupling of fluoroacetamides with boronic acids, under base-free conditions, to selectively give valuable α,α-d...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8688600cf5140ceb6904198dfc199cfd
https://hal.archives-ouvertes.fr/hal-03007624
https://hal.archives-ouvertes.fr/hal-03007624