Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marie Jose Egron"'
Autor:
Nathalie Mignet, Daniel Scherman, Marie Jose Egron, Nicolas Leforestier, Alain Quenot, Françoise Leclercq, Barbara Wetzer, Jean Herscovici
Publikováno v:
Organic Letters. 3:1893-1896
[see structure]. We report the synthesis of new cationic lipids. These amphiphiles present a hydrophobic domain connected to a guanidinium entity by an unsaturated glycoside scaffold. The synthetic strategy using amide or acetal linkage led to variou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82259636fd2f8bcdfc9755681bc5d251
https://doi.org/10.1021/ol0159423
https://doi.org/10.1021/ol0159423
Autor:
Jesse Paterson, Kostas Antonakis, Clara Uriel, Jean Herscovici, Moulay A. Alaoui-Jamali, Marie-Jose Egron
Publikováno v:
Antimicrobial Agents and Chemotherapy. 42:779-784
We compared the biological activity of a new group of keto-C-glycosides to that of a narrow spectrum of unsaturated ketonucleosides in a panel of non-small-cell lung cancer (NSCLC) cells with various levels of intrinsic resistance to standard chemoth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fb7e9b6add07aee84c8d4ec9f30091f
https://doi.org/10.1128/aac.42.4.779
https://doi.org/10.1128/aac.42.4.779
Publikováno v:
ChemInform. 22
Condensation of thymine with diacetyl-D-xylal and triacetyl-D-glucal afforded the unsaturated nucleosides 1, 6 and 7. After deacetylation and selective protection of the primary hydroxy groups in the case of the glucose derivatives, these compounds w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dda27551e844c656a0a8105730d7e46d
https://doi.org/10.1002/chin.199108321
https://doi.org/10.1002/chin.199108321
Autor:
Marie Jose Egron, Barbara Wetzer, Nathalie Mignet, Alain Quenot, Jean Herscovici, Daniel Scherman, Françoise Leclercq, Nicolas Leforestier
Publikováno v:
ChemInform. 32
We report the synthesis of new cationic lipids. These amphiphiles present a hydrophobic domain connected to a guanidinium entity by an unsaturated glycoside scaffold. The synthetic strategy using amide or acetal linkage led to various mono- and bicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03b665edafe56c4a49ca8c9a38e46556
https://doi.org/10.1002/chin.200150206
https://doi.org/10.1002/chin.200150206
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :3035-3039
Condensation of thymine with diacetyl-D-xylal and triacetyl-D-glucal afforded the unsaturated nucleosides 1, 6 and 7. After deacetylation and selective protection of the primary hydroxy groups in the case of the glucose derivatives, these compounds w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02742cd79291565808443294de09b2c6
https://doi.org/10.1039/p19900003035
https://doi.org/10.1039/p19900003035
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1219-1226
Amino hexopyranose nucleosides were prepared by treatment of the keto group with hydroxylamine hydrochloride followed by acetylation of the resulting oxime. Among other reagents, sodium borohydride–nickel chloride or sodium borohydride–molybdenum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8376357755650c079708bac50feff593
https://doi.org/10.1039/p19880001219
https://doi.org/10.1039/p19880001219
Publikováno v:
ChemInform. 19
Amino hexopyranose nucleosides were prepared by treatment of the keto group with hydroxylamine hydrochloride followed by acetylation of the resulting oxime. Among other reagents, sodium borohydride–nickel chloride or sodium borohydride–molybdenum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff4d001397bfa6c74e3a3c6a3f24f0e0
https://doi.org/10.1002/chin.198834340
https://doi.org/10.1002/chin.198834340