AAAAAA

   
Results: 1-15 |
Results: 15

Authors: Belloli, E Foulon, C Yous, S Vaccher, MP Bonte, JP Vaccher, C
Citation: E. Belloli et al., Direct separation of the stereoisomers of methoxytetrahydronaphthalene derivatives, new agonist and antagonist ligands for melatonin receptors, by liquid chromatography on cellulose chiral stationary phases, J CHROMAT A, 907(1-2), 2001, pp. 101-113

Authors: Lipka-Belloli, E Guelzim, A Yous, S Lefebvre, J Descamps-Francois, C Capet, F Vaccher, C
Citation: E. Lipka-belloli et al., Melatonin receptor agents: Synthesis, resolution by HPLC on polysaccharides chiral stationary phases, absolute configuration, and pharmacology of theenantiomers of (+/-)-N-[2-(7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)ethyl]acetamide, CHIRALITY, 13(4), 2001, pp. 199-206

Authors: Guelzim, A Belloli, E Yous, S Vaccher, C
Citation: A. Guelzim et al., Absolute configuration of N-[(-)-2-(7-methoxy-1,2,3,4-tetra- hydro-1-naphthyl)ethyl]cyclopropyl-carboxamide, a highly potent and selective melatonin analogue, ACT CRYST C, 57, 2001, pp. 100-101

Authors: Yous, S Klupsch, F Lesieur, I
Citation: S. Yous et al., Synthesis of 2(3H)-benzoxazolinone derivatives as potential melatonin receptor ligands, ORG PREP PR, 33(1), 2001, pp. 75-80

Authors: Chavatte, P Yous, S Lesieur, D Henichart, JP
Citation: P. Chavatte et al., Conformational analysis of tripeptide Ac-Lys-Pro-Val-NH2, COOH-terminal sequence of alpha-MSH, J PHARM PHA, 53(7), 2001, pp. 949-953

Authors: Chavatte, P Yous, S Marot, C Baurin, N Lesieur, D
Citation: P. Chavatte et al., Three-dimensional quantitative structure-activity relationships of cyclo-oxygenase-2 (COX-2) inhibitors: A comparative molecular field analysis, J MED CHEM, 44(20), 2001, pp. 3223-3230

Authors: Delhomel, JF Yous, S Depreux, P Lesieur, D
Citation: Jf. Delhomel et al., Synthesis of 2(3H)-benzoxazolone and 2(3H)-benzothiazolone derivatives as potential beta-3-adrenergic receptor ligands (part 2), J HETERO CH, 38(3), 2001, pp. 633-639

Authors: Belloli, E Foulon, C Yous, S Bonte, JP Vaccher, C
Citation: E. Belloli et al., Diastereomeric and enantiomeric resolution of methoxytetrahydronaphthalenederivatives, melatonin ligand receptors, by HPLC on amylose chiral stationary phases, CHROMATOGR, 53(3-4), 2001, pp. 216-219

Authors: Carato, P Yous, S Depreux, P
Citation: P. Carato et al., Synthesis of 6-chloromethyl benzothiazolin-2-one and of 6-chloromethyl benzoxazolin-2-one, ORG PREP PR, 32(1), 2000, pp. 69-74

Authors: Le Bourdonnec, B Meulon, E Yous, S Goossens, JF Houssin, R Henichart, JP
Citation: B. Le Bourdonnec et al., Synthesis and pharmacological evaluation of new pyrazolidine-3,5-diones asAT(1) angiotensin II receptor antagonists, J MED CHEM, 43(14), 2000, pp. 2685-2697

Authors: Le Bourdonnec, B Meulon, E Yous, S Houssin, R Henichart, JP
Citation: B. Le Bourdonnec et al., A new synthesis of N-alkyl pyrazolidine-3,5-diones and tetrahydropyridazine-3,6-diones, J HETERO CH, 37(5), 2000, pp. 1209-1212

Authors: Liacha, M Yous, S Depreux, P Poupaert, JH Lesieur, D
Citation: M. Liacha et al., Synthesis of N-(4,6-dimethylpyridin-2-yl)-benzoxazolinonyl methylcarboxamides with potential antiinflammatory activity, HETEROCYCLE, 51(8), 1999, pp. 1929-1943

Authors: Liacha, M Yous, S Poupaert, JH Depreux, P Aichaoui, H
Citation: M. Liacha et al., Friedel-Crafts acylation of 2(3H)-benzoxazolone: Investigation of the roleof the catalyst and microwave activation, MONATS CHEM, 130(11), 1999, pp. 1393-1397

Authors: Delhomel, JF Yous, S Depreux, P Lesieur, D
Citation: Jf. Delhomel et al., Synthesis of 2(3H)-benzoxazolinone derivatives as potential beta-3-adrenergic receptor ligands, J HETERO CH, 36(5), 1999, pp. 1241-1245

Authors: Roche, S Yous, S Couturier, D Rigo, B
Citation: S. Roche et al., On the reaction of Meldrum's acid with N-trimethylsilylanilines substituted by electron withdrawing groups, J HETERO CH, 36(4), 1999, pp. 1073-1075
Risultati: 1-15 |