Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Martine Fayolle"'
Autor:
Salia Tangara, Christian Philouze, Jean-Bernard Behr, Sandrine Py, Alice Kanazawa, Martine Fayolle, Jean-François Poisson
Publikováno v:
New Journal of Chemistry. 42:16735-16743
The synthesis of the peracetylated ketonitrone 4 is described in four steps from L-sorbose. This cyclic nitrone is crystalline and proved to preferentially adopt a 4H3 conformation with all acetate groups in pseudo-axial orientation. Nitrone 4 underg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e14ad0ec1e294e1b3658bbf91e1343a0
https://doi.org/10.1039/c8nj03868f
https://doi.org/10.1039/c8nj03868f
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 16:1267-1271
A series of 3-O-substituted glucose derivatives was prepared with alkyl, alkenyl, aromatic and ferrocenic substituents; to vary lipophilicity and hydrogen bonding ethylenedioxy and perfluorinated fragments were also introduced. Apparent affinities fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef258ac0a01e24d4f69cfe48c1b8e639
https://doi.org/10.1016/j.bmcl.2005.11.068
https://doi.org/10.1016/j.bmcl.2005.11.068
Publikováno v:
European Journal of Organic Chemistry. 2003:54-62
The Michael addition of bis(nitrogen or sulfur) nucleophiles to divinyl sulfone provides the corresponding macrocyclic adducts in good yields. The structures of some new macrocyclic sulfones are established by X-ray crystallographic analysis and NMR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cb5f292fa11c3d2f64836e838762f99
https://doi.org/10.1002/1099-0690(200301)2003:1<54::aid-ejoc54>3.0.co
https://doi.org/10.1002/1099-0690(200301)2003:1<54::aid-ejoc54>3.0.co
Autor:
Katja Becker, Christophe Morin, Tatiana Besset, Margit Brückner, Martine Fayolle, Elisabeth Davioud-Charvet, Danièle Limosin, Jean-Claude Moutet
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2008, 6 (15), pp.2731. ⟨10.1039/B802649C⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, Royal Society of Chemistry, 2008, 6 (15), pp.2731. ⟨10.1039/B802649C⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2008, 6 (15), pp.2731. ⟨10.1039/B802649C⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, Royal Society of Chemistry, 2008, 6 (15), pp.2731. ⟨10.1039/B802649C⟩
Various aza-analogues of 1,4-naphthoquinone and menadione were prepared and tested as inhibitors and substrates of the plasmodial thioredoxin and glutathione reductases as well as the human glutathione reductase. The replacement of one to two carbons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b3c3215aea907f809a28d973cb51252
https://hal-normandie-univ.archives-ouvertes.fr/hal-02541797
https://hal-normandie-univ.archives-ouvertes.fr/hal-02541797
