Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yohann Berhault"'
Autor:
Reynald Mangeant, Valérie Collot, Yohann Berhault, Thomas Cailly, Silvia Stiebing, Frédéric Fabis, Gonzalo Vera
Publikováno v:
Advanced Synthesis & Catalysis. 363:5099-5105
Autor:
Yohann Berhault, Marie Jouanne, Ikram Slimani, Charline Kieffer, Anne Sophie Voisin-Chiret, Rémi Legay, Jana Sopkova-de Oliveira Santos, Sylvain Rault, Victor Babin
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2017, 73 (37), pp.5509-5516. ⟨10.1016/j.tet.2017.07.049⟩
Tetrahedron, Elsevier, 2017, 73 (37), pp.5509-5516. ⟨10.1016/j.tet.2017.07.049⟩
International audience; We present Csingle bondH heteroarylation reactions between thiophene and variously substituted bromopyridines. The objective was to synthesize unsymmetrical 2,5-bipyridylthiophenes. We studied the reaction conditions allowing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1182640ee526eae33da30b417b2319d0
https://hal.archives-ouvertes.fr/hal-02043719
https://hal.archives-ouvertes.fr/hal-02043719
Autor:
Christine Fossey, Yohann Berhault, Silvia Stiebing, Valérie Collot, Frédéric Fabis, Bao Vy Lam, Thomas Cailly
Publikováno v:
ChemInform. 47
A unique route to highly functionalized indazoles is described. A regioselective magnesiation at position 3 of 4-, 5-, 6- and 7-iodo-2-THP-indazoles (THP=tetrahydropyranyl) has been developed using TMPMgCl⋅LiCl (TMP=2,2,6,6-tetramethylpiperidyl). T
Autor:
Frédéric Fabis, Yohann Berhault, Thomas Cailly, Silvia Stiebing, Bao Vy Lam, Valérie Collot, Christine Fossey
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2016, 22 (13), pp.4440-4446. ⟨10.1002/chem.201504828⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2016, 22 (13), pp.4440-4446. ⟨10.1002/chem.201504828⟩
International audience; A unique route to highly functionalized indazoles is described. A regioselective magnesiation at position 3 of 4-, 5-, 6- and 7-iodo-2-THP-indazoles (THP=tetrahydropyranyl) has been developed using TMPMgCl⋅LiCl (TMP=2,2,6,6-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d988b624d2b046d59b9557dd9ba6f8f6
https://hal.archives-ouvertes.fr/hal-02043771
https://hal.archives-ouvertes.fr/hal-02043771
Publikováno v:
ChemInform. 46
A direct amide bond synthesis between carbocyclic acids and amines is achieved in the presence of a highly active bench-stable catalyst.
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2015, 80 (9), pp.4532-4544. ⟨10.1021/acs.joc.5b00378⟩
Journal of Organic Chemistry, American Chemical Society, 2015, 80 (9), pp.4532-4544. ⟨10.1021/acs.joc.5b00378⟩
International audience; An efficient method has been developed for direct amide bond synthesis between carboxylic acids and amines via (2-(thiophen-2-ylmethyl)phenyl)boronic acid as a highly active bench-stable catalyst. This catalyst was found to be