Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Aurélie Lemétais"'
Autor:
Mathieu Carlier, Emilie Lesur, Aurélie Baron, Aurélie Lemétais, Karine Guitot, Loïc Roupnel, Christiane Dietrich, Gilles Doisneau, Dominique Urban, Nicolas Bayan, Jean-Marie Beau, Dominique Guianvarc'h, Boris Vauzeilles, Yann Bourdreux
Publikováno v:
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2022, 20 (9), pp.1974-1981. ⟨10.1039/D2OB00107A⟩
Organic & Biomolecular Chemistry, 2022, 20 (9), pp.1974-1981. ⟨10.1039/D2OB00107A⟩
Trehalose-based probes are useful tools that allow the detection of the mycomembrane of mycobacteria through the metabolic labeling approach. Trehalose analogues conjugated to fluorescent probes can be used, and other probes are functionalized with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23b5548bbcdb982416bdbbf7a2324001
https://hal.science/hal-03801948/document
https://hal.science/hal-03801948/document
Publikováno v:
European Journal of Organic Chemistry. 2017:3355-3361
Regioselective differentiation of the hydroxy groups of mono- and oligosaccharide substrates is necessary to form building blocks that can be used for synthetic transformations. In this paper, we show that iron(III) chloride hexahydrate catalyses the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4b73826dc6f4b036907036855e1cdb7
https://doi.org/10.1002/ejoc.201700538
https://doi.org/10.1002/ejoc.201700538
Autor:
Marco Lepore, Germain Puzo, Jacques Prandi, Jean-Marie Beau, Aurélie Lemétais, Lucia Mori, Benjamin Gau, Gennaro De Libero, Yann Bourdreux, Luis F. Garcia-Alles, Martine Gilleron
Publikováno v:
ChemBioChem
ChemBioChem, Wiley-VCH Verlag, 2013, 14 (18), pp.2413-2417. ⟨10.1002/cbic.201300482⟩
ChemBioChem, Wiley-VCH Verlag, 2013, 14 (18), pp.2413-2417. ⟨10.1002/cbic.201300482⟩
International audience; The longer, the better: Increasing the lengths of the 1,3-methyl-branched fatty acyl chain units in mycobacterial diacylated sulfoglycolipid (Acyl2 SGL) analogues led to dramatic improvements in their antigenic properties and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d25d886d8c201c6aa8d1ce2c97005973
https://doi.org/10.1002/cbic.201300482
https://doi.org/10.1002/cbic.201300482
Autor:
Amandine Xolin, Gilles Doisneau, Aurélie Mathieu, Aurélie Lemétais, Jean-François Soulé, Jean-Marie Beau, Boris Vauzeilles, François-Didier Boyer, Stephanie Norsikian, Dominique Urban, Arnaud Stévenin, Alexandra Gouasmat, Yann Bourdreux
This review particularly emphasizes synthetic applications resulting from cascade or one-pot transformations and a glycosylation reaction promoted by ferric salts. These easy to handle, cheap and environment-friendly salts have been examined for thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af4ab7f48ed5a3bfffaf73e47163aff7
https://doi.org/10.1039/9781849739986-00118
https://doi.org/10.1039/9781849739986-00118
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2013, 78 (15), pp.7648-57. ⟨10.1021/jo4012255⟩
Journal of Organic Chemistry, American Chemical Society, 2013, 78 (15), pp.7648-57. ⟨10.1021/jo4012255⟩
International audience; Tetra-O-acylated sulfolipids are metabolites found in the cell wall of Mycobacterium tuberculosis, the causative agent of tuberculosis. Their role in pathogenesis remains, however, undefined. Here we describe a novel access to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fec29f850ac864dfca65994c263bf0bc
https://hal.archives-ouvertes.fr/hal-00910978
https://hal.archives-ouvertes.fr/hal-00910978
Publikováno v:
ChemInform. 42
The successful introduction of orthogonal protecting groups into glucose, maltose, and trehalose derivatives is elaborated using the iron-catalyzed tandem reductive etherification—acetylation of persilylated carbohydrates with benzaldehyde in the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::900f6e94bbc48b3ee55648e43068098e
https://doi.org/10.1002/chin.201124190
https://doi.org/10.1002/chin.201124190
Publikováno v:
Chemical Communications. 47:2146
Tandem catalysis by using iron(III) chloride hexahydrate leads to carbohydrate building blocks displaying an orthogonal protecting group pattern as illustrated by the regioselective protection of trehalose and maltose disaccharides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6056ea3b3669418197a77edd0212359
https://doi.org/10.1039/c0cc04398b
https://doi.org/10.1039/c0cc04398b
Autor:
Gouasmat, Alexandra1, Lemétais, Aurélie1, Solles, Julien1, Bourdreux, Yann1 yann.bourdreux@u‐psud.fr, Beau, Jean‐Marie1,2 jean‐marie.beau@u‐psud.fr
Publikováno v:
European Journal of Organic Chemistry. 6/23/2017, Vol. 2017 Issue 23, p3355-3361. 7p. 6 Diagrams.
Autor:
Carlier, Mathieu, Lesur, Emilie, Baron, Aurélie, Lemétais, Aurélie, Guitot, Karine, Roupnel, Loïc, Dietrich, Christiane, Doisneau, Gilles, Urban, Dominique, Bayan, Nicolas, Beau, Jean-Marie, Guianvarc'h, Dominique, Vauzeilles, Boris, Bourdreux, Yann
Publikováno v:
Organic & Biomolecular Chemistry; 3/7/2022, Vol. 20 Issue 9, p1974-1981, 8p
Autor:
Gau, Benjamin, Lemétais, Aurélie, Lepore, Marco, Garcia‐Alles, Luis Fernando, Bourdreux, Yann, Mori, Lucia, Gilleron, Martine, De Libero, Gennaro, Puzo, Germain, Beau, Jean‐Marie, Prandi, Jacques
Publikováno v:
ChemBioChem; Dec2013, Vol. 14 Issue 18, p2413-2417, 5p