Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Stéphane Sengmany"'
Autor:
Sébastien Bouvet, Bruce Pégot, Stéphane Sengmany, Erwan Le Gall, Eric Léonel, Anne-Marie Goncalves, Emmanuel Magnier
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 2948-2953 (2020)
The electroreduction of SF6 is shown at ambient temperature in acetonitrile using an array of platinum microelectrodes to improve the electrical detection. Its half reduction potential occurs at −2.17 V vs Fc+/Fc. The exact number of electrons for
Externí odkaz:
https://doaj.org/article/619b20c179dd4a72b01484c92e53f49a
Publikováno v:
Molecules, Vol 16, Iss 7, Pp 5550-5560 (2011)
A range of novel 4-amino-6-arylpyrimidines has been prepared under mild conditions by an electrochemical reductive cross-coupling between 4-amino-6-chloro-pyrimidines and functionalized aryl halides. The process, which employs a sacrificial iron anod
Externí odkaz:
https://doaj.org/article/79b895b4db9c4e50a1c6f4ffd6f68ef6
Publikováno v:
The Journal of organic chemistry.
Arylamines represent a class of compounds widely found in natural products and pharmaceuticals. Among methodologies devoted to their synthesis, nickel-catalyzed amination of aryl halides constitutes one of the most employed conventional strategies. H
Autor:
Eric Léonel, Abdelhakim Ouarti, Ibtihal Kribii, Farah Daili, Stéphane Sengmany, Marine Pinaud, Erwan Le Gall
Publikováno v:
European Journal of Organic Chemistry. 2020:3452-3455
Publikováno v:
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2021, 2021 (17), pp.2462-2469. ⟨10.1002/ejoc.202100194⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2021, 2021 (17), pp.2462-2469. ⟨10.1002/ejoc.202100194⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c5267999c35b02251311252281e9ef8
https://hal.archives-ouvertes.fr/hal-03219164
https://hal.archives-ouvertes.fr/hal-03219164
Autor:
Eric Léonel, Morgane Rousselle, Didier Dubreuil, Gervaise Loirand, Florian Dilasser, Rémy Le Guével, Erwan Le Gall, Muriel Pipelier, Vincent Sauzeau, Stéphane Sengmany, Jacques Lebreton, Mathilde Sitter, Thierry Martens
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic and Medicinal Chemistry Letters, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic & Medicinal Chemistry Letters
Bioorganic & Medicinal Chemistry Letters, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic and Medicinal Chemistry Letters, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic & Medicinal Chemistry Letters
Bioorganic & Medicinal Chemistry Letters, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
International audience; Various 3-amino-, 3-aryloxy- and alkoxy-6-arylpyridazines have been synthesized by an electrochemical reductive cross-coupling between 3-amino-, 3-aryloxy- or 3-alkoxy-6-chloropyridazines and aryl or heteroaryl halides. In vit
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2020, 31 (12), pp.1191-1196. ⟨10.1055/s-0039-1690899⟩
SYNLETT, Georg Thieme Verlag, 2020, 31 (12), pp.1191-1196. ⟨10.1055/s-0039-1690899⟩
Mild experimental conditions for a direct phosphonylation of an easily cleavable N-carbamate-tetrahydroisoquinoline have been described under constant current electrolysis. The developed electrochemical process allowed to prepare α-aminophosphonates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdda62b902d471e1779534d34a799ff3
https://hal.archives-ouvertes.fr/hal-03129621
https://hal.archives-ouvertes.fr/hal-03129621
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2017, 50 (01), pp.146-154. ⟨10.1055/s-0036-1589100⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, Georg Thieme Verlag, 2017, 50 (01), pp.146-154. ⟨10.1055/s-0036-1589100⟩
SYNTHESIS, Georg Thieme Verlag, 2017, 50 (01), pp.146-154. ⟨10.1055/s-0036-1589100⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, Georg Thieme Verlag, 2017, 50 (01), pp.146-154. ⟨10.1055/s-0036-1589100⟩
Due to their widespread presence in functional materials and pharmaceuticals, biaryls are of fundamental importance in organic chemistry. Methods for the synthesis of symmetrical biaryls generally involve both metallic reduction and transition-metal
Publikováno v:
European Journal of Organic Chemistry. 2016:4865-4871
The rarely described 4-(hetero)aryl-6-pyrrolylpyrimidines are prepared by electroreductive nickel-catalysed cross-coupling reactions between aryl halides and chloropyrimidines. Inherent predictable issues of such metal-catalysed reactions that involv
Publikováno v:
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, Royal Society of Chemistry, 2018, 16 (24), pp.4495-4500. ⟨10.1039/c8ob00500a⟩
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2018, 16 (24), pp.4495-4500. ⟨10.1039/c8ob00500a⟩
Organic & Biomolecular Chemistry, Royal Society of Chemistry, 2018, 16 (24), pp.4495-4500. ⟨10.1039/c8ob00500a⟩
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2018, 16 (24), pp.4495-4500. ⟨10.1039/c8ob00500a⟩
The electrochemically-assisted synthesis of (hetero)arylphosphonates from (hetero)aryl halides and dimethyl phosphite is described. Very mild and simple conditions are employed as the cross-coupling is carried out in galvanostatic mode, in an undivid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afe2fc81ab7f94fd8ab2b5ffec0feaaf
https://hal.archives-ouvertes.fr/hal-03129533
https://hal.archives-ouvertes.fr/hal-03129533