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Results: 1-19 |
Results: 19
1,3-DIPOLAR CYCLOADDITION REACTIONS OF 4-SILACYCLOHEX(HEPT)-2-EN-1-ONE DERIVATIVES - SYNTHESIS OF NOVEL AZASILABICYCLIC COMPOUNDS
Authors: DAMOUR D BARREAU M FARDIN V DHALEINE F VUILHORGNE M MIGNANI S
Citation: D. Damour et al., 1,3-DIPOLAR CYCLOADDITION REACTIONS OF 4-SILACYCLOHEX(HEPT)-2-EN-1-ONE DERIVATIVES - SYNTHESIS OF NOVEL AZASILABICYCLIC COMPOUNDS, Synlett, (2), 1998, pp. 153
A CONVENIENT SYNTHETIC ENTRY INTO 7-AZA-2,2-DIPHENYL-2-SILABICYCLO[3.3.0] OCTANE DERIVATIVES
Authors: DAMOUR D DHALEINE F MORGAT A VUILHORGNE M MIGNANI S
Citation: D. Damour et al., A CONVENIENT SYNTHETIC ENTRY INTO 7-AZA-2,2-DIPHENYL-2-SILABICYCLO[3.3.0] OCTANE DERIVATIVES, Heterocycles, 45(9), 1997, pp. 1805-1808
WITH RESPECT TO RECOMBINANT PROTEINS
Authors: MONEGIER B CLERC FF FAUCHER D VUILHORGNE M
Citation: B. Monegier et al., WITH RESPECT TO RECOMBINANT PROTEINS, Biofutur, (164), 1997, pp. 8-10
DEGRADATION PATHWAYS OF SALMON-CALCITONIN IN AQUEOUS-SOLUTION
Authors: WINDISCH V DELUCCIA F DUHAU L HERMAN F MENCEL JJ TANG SY VUILHORGNE M
Citation: V. Windisch et al., DEGRADATION PATHWAYS OF SALMON-CALCITONIN IN AQUEOUS-SOLUTION, Journal of pharmaceutical sciences, 86(3), 1997, pp. 359-364
DESIGN, SYNTHESIS AND BINDING AFFINITIES OF NOVEL NONPEPTIDE MIMICS OF SOMATOSTATIN SANDOSTATIN(R)/
Authors: DAMOUR D BARREAU M BLANCHARD JC BURGEVIN MC DOBLE A HERMAN F PANTEL G JAMESSURCOUF E VUILHORGNE M MIGNANI S POITOUT L LEMERRER Y DEPEZAY JC
Citation: D. Damour et al., DESIGN, SYNTHESIS AND BINDING AFFINITIES OF NOVEL NONPEPTIDE MIMICS OF SOMATOSTATIN SANDOSTATIN(R)/, Bioorganic & medicinal chemistry letters, 6(14), 1996, pp. 1667-1672
RADICAL-INDUCED CYCLIZATIONS OF 1-SILA-CYCLOPENT-2-ENE DERIVATIVES - SYNTHESIS OF NOVEL AZASILABICYCLIC COMPOUNDS
Authors: DAMOUR D BARREAU M DHALEINE F DOERFLINGER G VUILHORGNE M MIGNANI S
Citation: D. Damour et al., RADICAL-INDUCED CYCLIZATIONS OF 1-SILA-CYCLOPENT-2-ENE DERIVATIVES - SYNTHESIS OF NOVEL AZASILABICYCLIC COMPOUNDS, Synlett, (9), 1996, pp. 890
SEMISYNTHESIS OF RPR 121056A, A MAJOR METABOLITE OF IRINOTECAN (CPT-11)
Authors: BOURZAT JD VUILHORGNE M RIVORY LP ROBERT J COMMERCON A
Citation: Jd. Bourzat et al., SEMISYNTHESIS OF RPR 121056A, A MAJOR METABOLITE OF IRINOTECAN (CPT-11), Tetrahedron letters, 37(35), 1996, pp. 6327-6330
IDENTIFICATION AND PROPERTIES OF A MAJOR PLASMA METABOLITE OF IRINOTECAN (CPT-11) ISOLATED FROM THE PLASMA OF PATIENTS
Authors: RIVORY LP RIOU JF HAAZ MC SABLE S VUILHORGNE M COMMERCON A POND SM ROBERT J
Citation: Lp. Rivory et al., IDENTIFICATION AND PROPERTIES OF A MAJOR PLASMA METABOLITE OF IRINOTECAN (CPT-11) ISOLATED FROM THE PLASMA OF PATIENTS, Cancer research, 56(16), 1996, pp. 3689-3694
VITAMIN-B12 - HOW THE PROBLEM OF ITS BIOSYNTHESIS WAS SOLVED
Authors: BLANCHE F CAMERON B CROUZET J DEBUSSCHE L THIBAUT D VUILHORGNE M LEEPER FJ BATTERSBY AR
Citation: F. Blanche et al., VITAMIN-B12 - HOW THE PROBLEM OF ITS BIOSYNTHESIS WAS SOLVED, Angewandte Chemie, International Edition in English, 34(4), 1995, pp. 383-411
UNUSUAL TRANSFORMATION OF THE 3-HYDROXY-PICOLINOYL RESIDUE OF PRISTINAMYCIN I-A
Authors: PARIS JM FRANCOIS J MOLHERAT C ALBANO F ROBIN M VUILHORGNE M BARRIERE JC
Citation: Jm. Paris et al., UNUSUAL TRANSFORMATION OF THE 3-HYDROXY-PICOLINOYL RESIDUE OF PRISTINAMYCIN I-A, Journal of antibiotics, 48(7), 1995, pp. 676-682
RPR113228, A NOVEL FARNESYL-PROTEIN TRANSFERASE INHIBITOR PRODUCED BYCHRYSOSPORIUM-LOBATUM
Authors: VANDERPYL D CANS P DEBERNARD JJ HERMAN F LELIEVRE Y TAHRAOUI L VUILHORGNE M LEBOUL J
Citation: D. Vanderpyl et al., RPR113228, A NOVEL FARNESYL-PROTEIN TRANSFERASE INHIBITOR PRODUCED BYCHRYSOSPORIUM-LOBATUM, Journal of antibiotics, 48(7), 1995, pp. 736-737
PRIMARY STRUCTURE CONTROL OF RECOMBINANT PROTEINS USING HIGHPERFORMANCE LIQUID-CHROMATOGRAPHY, MASS-SPECTROMETRY AND MICROSEQUENCING
Authors: CLERC FF MONEGIER B FAUCHER D CUINE F POURCET C HOLT JC TANG SY VANDORSSELAER A BECQUART J VUILHORGNE M
Citation: Ff. Clerc et al., PRIMARY STRUCTURE CONTROL OF RECOMBINANT PROTEINS USING HIGHPERFORMANCE LIQUID-CHROMATOGRAPHY, MASS-SPECTROMETRY AND MICROSEQUENCING, Journal of chromatography B. Biomedical applications, 662(2), 1994, pp. 245-259
IMPROVED ACCESS TO 19-NOR-7-BETA,8-BETA-METHYLENE-TAXOIDS AND FORMATION OF A 7-MEMBERED C-RING ANALOG OF DOCETAXEL BY ELECTROCHEMISTRY
Authors: BOUCHARD H PULICANI JP VUILHORGNE M BOURZAT JD COMMERCON A
Citation: H. Bouchard et al., IMPROVED ACCESS TO 19-NOR-7-BETA,8-BETA-METHYLENE-TAXOIDS AND FORMATION OF A 7-MEMBERED C-RING ANALOG OF DOCETAXEL BY ELECTROCHEMISTRY, Tetrahedron letters, 35(52), 1994, pp. 9713-9716
PREPARATION OF DES-3-HYDROXY-PICOLINOYL PRISTINAMYCINS-I
Authors: BARRIERE JC BACQUE E PARIS JM ALBANO F FRANCOIS J MOLHERAT C VUILHORGNE M
Citation: Jc. Barriere et al., PREPARATION OF DES-3-HYDROXY-PICOLINOYL PRISTINAMYCINS-I, Tetrahedron letters, 35(51), 1994, pp. 9565-9568
STRUCTURES OF THE MAJOR HUMAN METABOLITES OF DOCETAXEL (RP 56976-TAXOTERE(R))
Authors: MONEGIER B GAILLARD C SABLE S VUILHORGNE M
Citation: B. Monegier et al., STRUCTURES OF THE MAJOR HUMAN METABOLITES OF DOCETAXEL (RP 56976-TAXOTERE(R)), Tetrahedron letters, 35(22), 1994, pp. 3715-3718
PARTIAL SYNTHESIS OF MAJOR HUMAN METABOLITES OF DOCETAXEL
Authors: COMMERCON A BOURZAT JD BEZARD D VUILHORGNE M
Citation: A. Commercon et al., PARTIAL SYNTHESIS OF MAJOR HUMAN METABOLITES OF DOCETAXEL, Tetrahedron, 50(34), 1994, pp. 10289-10298
ELECTROCHEMICAL REDUCTION OF PRISTINAMYCIN I-A AND RELATED STREPTOGRAMINS IN AQUEOUS ACIDIC MEDIUM
Authors: LARGERON M VUILHORGNE M LEPOTIER I AUZEIL N BACQUE E PARIS JM FLEURY MB
Citation: M. Largeron et al., ELECTROCHEMICAL REDUCTION OF PRISTINAMYCIN I-A AND RELATED STREPTOGRAMINS IN AQUEOUS ACIDIC MEDIUM, Tetrahedron, 50(21), 1994, pp. 6307-6332
THE ORIGIN OF THE DIVERSITY OF CROTOXIN ISOFORMS IN THE VENOM OF CROTALUS-DURISSUS-TERRIFICUS
Authors: FAURE G CHOUMET V BOUCHIER C CAMOIN L GUILLAUME JL MONEGIER B VUILHORGNE M BON C
Citation: G. Faure et al., THE ORIGIN OF THE DIVERSITY OF CROTOXIN ISOFORMS IN THE VENOM OF CROTALUS-DURISSUS-TERRIFICUS, European journal of biochemistry, 223(1), 1994, pp. 161-164
SOLUTION STRUCTURE OF RP-71955, A NEW 21 AMINO-ACID TRICYCLIC PEPTIDEACTIVE AGAINST HIV-1 VIRUS
Authors: FRECHET D GUITTON JD HERMAN F FAUCHER D HELYNCK G DUSORBIER BM RIDOUX JP JAMESSURCOUF E VUILHORGNE M
Citation: D. Frechet et al., SOLUTION STRUCTURE OF RP-71955, A NEW 21 AMINO-ACID TRICYCLIC PEPTIDEACTIVE AGAINST HIV-1 VIRUS, Biochemistry, 33(1), 1994, pp. 42-50
Risultati: 1-19 |