Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tourin Bzeih"'
Publikováno v:
European Journal of Organic Chemistry. 2019:2602-2611
A new metal-free procedure allowing a Csp 3-N bond formation through coupling of pyridotriazoles and weakly nucleophilic anilines has been developed. This sustainable reaction shows high tolerance towards functional groups (ketones, free alcohols) le
Publikováno v:
Advanced Synthesis & Catalysis. 360:584-594
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, 2019, 84 (1), pp.228-238. ⟨10.1021/acs.joc.8b02623⟩
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (1), pp.228-238. ⟨10.1021/acs.joc.8b02623⟩
Journal of Organic Chemistry, 2019, 84 (1), pp.228-238. ⟨10.1021/acs.joc.8b02623⟩
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (1), pp.228-238. ⟨10.1021/acs.joc.8b02623⟩
International audience; A one-pot Barluenga coupling between N-tosylhydrazones and nitro-benzyl bromide, followed by deoxygenation of ortho-nitrostyrenes, and subsequent cyclization has been developed, providing a new way to synthesize various C2-ary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0629cfc8d708b02146ba1d03d0b83b1
https://hal.science/hal-02414153/document
https://hal.science/hal-02414153/document
Autor:
Ali Hachem, Mouad Alami, Timothée Naret, Jérôme Bignon, Ali Khalaf, Tourin Bzeih, Abdallah Hamze, Nada Jaber, Jean-Daniel Brion
Publikováno v:
Chemical Communications. 52:13027-13030
A convergent and effective synthesis of 3-aryl-indoles, 2,3-diaryl indoles, and (1-arylvinyl)carbazoles from a one-pot sequence involving the coupling of N-tosylhydrazones with ortho-nitro-haloarenes followed by a cyclization has been developed. Comp
Autor:
Tourin, Bzeih, Diana, Lamaa, Gilles, Frison, Ali, Hachem, Nada, Jaber, Jerome, Bignon, Pascal, Retailleau, Mouad, Alami, Abdallah, Hamze
Publikováno v:
Organic letters. 19(24)
A novel, sequential, palladium-catalyzed, cross-coupling reaction using N-tosylhydrazone and bromonitrobenzene derivatives followed by reductive cyclization has been developed. This transformation providing an efficient route to unexpected N-arylindo
Autor:
Ali Hachem, Diana Lamaa, Jérôme Bignon, Pascal Retailleau, Mouad Alami, Nada Jaber, Gilles Frison, Tourin Bzeih, Abdallah Hamze
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2017, 19 (24), pp.6700-6703. ⟨10.1021/acs.orglett.7b03422⟩
Organic Letters, American Chemical Society, 2017, 19 (24), pp.6700-6703. ⟨10.1021/acs.orglett.7b03422⟩
A novel, sequential, palladium-catalyzed, cross-coupling reaction using N-tosylhydrazone and bromonitrobenzene derivatives followed by reductive cyclization has been developed. This transformation providing an efficient route to unexpected N-arylindo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b1ceff30d8334d4be257b72736b13db
https://hal.archives-ouvertes.fr/hal-01673626
https://hal.archives-ouvertes.fr/hal-01673626