Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Laurent Giordano"'
Publikováno v:
Molecules, Vol 25, Iss 14, p 3292 (2020)
Natural products (NPs) constitute a significant source of active biomolecules widely used in medicine, pharmacology and cosmetics. However, NPs structural characterization has the drawback of their chemical instability during the extraction steps and
Externí odkaz:
https://doaj.org/article/45ee7480e9ff49c6b671e35934024e47
Publikováno v:
European Journal of Organic Chemistry. 2020:3351-3366
Autor:
A. Beal, Laurent Giordano, Rémy Fortrie, Jean-Valère Naubron, David Gatineau, Damien Hérault, Gérard Buono
Publikováno v:
Chirality
Chirality, 2022, 34 (1), pp.27-33. ⟨10.1002/chir.23383⟩
Chirality, 2022, 34 (1), pp.27-33. ⟨10.1002/chir.23383⟩
International audience; The racemization mechanism of tert-butyl-phenylphosphido-borane is investigated experimentally andtheoretically. Based on this converging approach, it is shown,first, that several phosphido-borane molecular speciescoexist at t
Publikováno v:
European Journal of Organic Chemistry. 2018:5427-5434
Autor:
Damien Bonne, Marion Jean, Nicolas Vanthuyne, Sara Chentouf, Jean Rodriguez, Xiaoze Bao, Jean-Valère Naubron, Laurent Giordano, Stéphane Humbel, Peng Liu
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, 2020, 142 (38), pp.16199-16204. ⟨10.1021/jacs.0c07995⟩
Journal of the American Chemical Society, American Chemical Society, 2020, 142 (38), pp.16199-16204. ⟨10.1021/jacs.0c07995⟩
Journal of the American Chemical Society, 2020, 142 (38), pp.16199-16204. ⟨10.1021/jacs.0c07995⟩
Journal of the American Chemical Society, American Chemical Society, 2020, 142 (38), pp.16199-16204. ⟨10.1021/jacs.0c07995⟩
International audience; An expedient synthesis of a new family of configurationally stable dioxa[6]helicenes was established using a sequential helicoselective organocatalyzed heteroannulation/eliminative aromatization via enantioenriched fused 2-nit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfeb51e58a3257807e9de9071b9a6d62
https://hal.science/hal-02953766/document
https://hal.science/hal-02953766/document
Autor:
Laurent Giordano, Delphine Moraleda, Sabine Michaud-Chevallier, Romain Membrat, Alexandre Vasseur, Alexandre Martinez, Didier Nuel
Publikováno v:
RSC Advances
RSC Advances, Royal Society of Chemistry, 2019, 9 (65), pp.37825-37829. ⟨10.1039/C9RA08709E⟩
RSC Advances, 2019, 9 (65), pp.37825-37829. ⟨10.1039/C9RA08709E⟩
RSC Advances, Royal Society of Chemistry, 2019, 9 (65), pp.37825-37829. ⟨10.1039/C9RA08709E⟩
RSC Advances, 2019, 9 (65), pp.37825-37829. ⟨10.1039/C9RA08709E⟩
Platinum–(phosphinito–phosphinous acid) complex catalyzes the oxidative fragmentation of hindered piperidinols according to a hydrogen transfer induced methodology. This catalyst acts successively as both a hydrogen carrier and soft Lewis acid in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5c4d7491d6efd447f53cd368dc0b6ba
https://hal.univ-lorraine.fr/hal-02373357
https://hal.univ-lorraine.fr/hal-02373357
Autor:
Romain Membrat, Didier Nuel, Sébastien Lemouzy, Damien Hérault, Enzo Olivieri, Laurent Giordano, Gérard Buono, Marion Jean, Muriel Albalat
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2019, pp.4551-4557. ⟨10.1021/acs.joc.9b00333⟩
Journal of Organic Chemistry, American Chemical Society, 2019, ⟨10.1021/acs.joc.9b00333⟩
Journal of Organic Chemistry, 2019, 84, pp.4551-4557. ⟨10.1021/acs.joc.9b00333⟩
Journal of Organic Chemistry, American Chemical Society, 2019, pp.4551-4557. ⟨10.1021/acs.joc.9b00333⟩
Journal of Organic Chemistry, American Chemical Society, 2019, ⟨10.1021/acs.joc.9b00333⟩
Journal of Organic Chemistry, 2019, 84, pp.4551-4557. ⟨10.1021/acs.joc.9b00333⟩
International audience; The synthesis of P-stereogenic aminophos-phine-boranes has been developed on the basis of umpolung reactivity of in situ generated alkylarylphosphido-boranes, which are normally configurationally unstable intermediates. In our
Publikováno v:
Asian Journal of Organic Chemistry
Asian Journal of Organic Chemistry, 2019, 8 (11), pp.2011-2016. ⟨10.1002/ajoc.201900529⟩
Asian Journal of Organic Chemistry, Wiley, 2019, 8 (11), pp.2011-2016. ⟨10.1002/ajoc.201900529⟩
Asian Journal of Organic Chemistry, 2019, 8 (11), pp.2011-2016. ⟨10.1002/ajoc.201900529⟩
Asian Journal of Organic Chemistry, Wiley, 2019, 8 (11), pp.2011-2016. ⟨10.1002/ajoc.201900529⟩
International audience; Cycloisomerization of 1,6‐enynes to access azabicyclo[4.1.0]heptenes was achieved in the presence of commercially available [RuCl2(CO)3]2 after a comprehensive study on the electronic properties of ruthenium complexes. A ser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53fc180eb50e928a92734403b319141d
https://hal.science/hal-02514511
https://hal.science/hal-02514511
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2019, 60 (3), pp.240-243. ⟨10.1016/j.tetlet.2018.12.020⟩
Tetrahedron Letters, 2019, 60 (3), pp.240-243. ⟨10.1016/j.tetlet.2018.12.020⟩
Tetrahedron Letters, Elsevier, 2019, 60 (3), pp.240-243. ⟨10.1016/j.tetlet.2018.12.020⟩
Tetrahedron Letters, 2019, 60 (3), pp.240-243. ⟨10.1016/j.tetlet.2018.12.020⟩
International audience; A convenient method to access a broad variety of N-alkyl-(2,2,6,6)-tetramethylpiperidin-4-ol compounds is reported. The thermal treatment of a mixture of (2,2,6,6)-tetramethylpiperidin-4-ol and allyl or benzyl bromide derivati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65174e3839c7ecca0b53c01e5001bffc
https://hal.univ-lorraine.fr/hal-01969189/file/RM_2019.pdf
https://hal.univ-lorraine.fr/hal-01969189/file/RM_2019.pdf