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Results: 1-18 |
Results: 18

Authors: Carangio, A McGuigan, C Cahard, D Andrei, G Snoeck, R De Clercq, E Balzarini, J
Citation: A. Carangio et al., Synthesis and in vitro evaluation of novel anti-varicella-zoster virus (VZV) nucleosides, NUCLEOS NUC, 20(4-7), 2001, pp. 653-656

Authors: Cahard, D Duhamel, P
Citation: D. Cahard et P. Duhamel, Alkoxide-mediated preparation of enolates from silyl enol ethers and enol acetates - From discovery to synthetic applications, EUR J ORG C, (6), 2001, pp. 1023-1031

Authors: Mohar, B Baudoux, M Plaquevent, JC Cahard, D
Citation: B. Mohar et al., Electrophilic fluorination mediated by cinchona alkaloids: Highly enantioselective synthesis of alpha-fluoro-alpha-plienylglycine derivatives, ANGEW CHEM, 40(22), 2001, pp. 4214-4216

Authors: Thierry, B Plaquevent, JC Cahard, D
Citation: B. Thierry et al., New polymer-supported chiral phase-transfer catalysts in the asymmetric synthesis of alpha-amino acids: the role of a spacer, TETRAHEDR-A, 12(7), 2001, pp. 983-986

Authors: Nshimyumukiza, P Cahard, D Rouden, J Lasne, MC Plaquevent, JC
Citation: P. Nshimyumukiza et al., Construction of functionalized/substituted bipyridines by means of Negishicross-coupling reactions. Formal synthesis of (+/-)-cytisine, TETRAHEDR L, 42(44), 2001, pp. 7787-7790

Authors: Cahard, D Audouard, C Plaquevent, JC Toupet, L Roques, N
Citation: D. Cahard et al., N-Fluorocinchonidinium tetrafluoroborate F-CD-BF4: purification and structure elucidation of this novel enantioselective electrophilic fluorinating agent, TETRAHEDR L, 42(10), 2001, pp. 1867-1869

Authors: Thierry, B Perrard, T Audouard, C Plaquevent, JC Cahard, D
Citation: B. Thierry et al., Solution- and solid-phase approaches in asymmetric phase-transfer catalysis by cinchona alkaloid derivatives, SYNTHESIS-S, (11), 2001, pp. 1742-1746

Authors: Allender, CJ Brain, KR Ballatore, C Cahard, D Siddiqui, A McGuigan, C
Citation: Cj. Allender et al., Separation of individual antiviral nucleotide prodrugs from synthetic mixtures using cross-reactivity of a molecularly imprinted stationary phase, ANALYT CHIM, 435(1), 2001, pp. 107-113

Authors: Cahard, D Audouard, C Plaquevent, JC Roques, N
Citation: D. Cahard et al., Design, synthesis, and evaluation of a novel class of enantioselective electrophilic fluorinating agents: N-fluoro ammonium salts of cinchona alkaloids (F-CA-BF4), ORG LETT, 2(23), 2000, pp. 3699-3701

Authors: Knaggs, MH McGuigan, C Harris, SA Heshmati, P Cahard, D Gilbert, IH Balzarini, J
Citation: Mh. Knaggs et al., A QSAR study investigating the effect of L-alanine ester variation on the anti-HIV activity of some phosphoramidate derivatives of d4T, BIOORG MED, 10(18), 2000, pp. 2075-2078

Authors: Aquaro, S Wedgwood, O Yarnold, C Cahard, D Pathinara, R McGuigan, C Calio', R De Clercq, E Balzarini, J Perno, CF
Citation: S. Aquaro et al., Activities of masked 2 ',3 '-dideoxynucleoside monophosphate derivatives against human immunodeficiency virus in resting macrophages, ANTIM AG CH, 44(1), 2000, pp. 173-177

Authors: Trancard, D Tout, JB Giard, T Chichaoui, I Cahard, D Plaquevent, JC
Citation: D. Trancard et al., Pyrrolidines bearing a quaternary alpha-stereogenic center. Part 2. Accessto proline chimeras, stereoselective approach and mechanistic aspects, TETRAHEDR L, 41(20), 2000, pp. 3843-3847

Authors: Cahard, D Mammeri, M Poirier, JM Duhamel, L
Citation: D. Cahard et al., A general synthesis of (2Z)-terpenoic acids, TETRAHEDR L, 41(19), 2000, pp. 3619-3622

Authors: Mechaly, I Krosniak, M Azay, J Cassanas, G Roque, C Cahard, D Serrano, JJ Cros, G
Citation: I. Mechaly et al., Interactive computerized microscopy as a tool for quantifying vascular remodelling - Effects of diabetes and V1a receptor antagonist SR 49059 on rat mesenteric arterial bed, J PHARM TOX, 41(2-3), 1999, pp. 59-67

Authors: Cahard, D Ferron, L Plaquevent, JC
Citation: D. Cahard et al., Carba-methylephedrine and carba-pseudo-methylephedrine as tools for probing the role of the nitrogen atom of chiral amino alcohols in asymmetric synthesis, SYNLETT, 1999, pp. 960-962

Authors: Saboulard, D Naesens, L Cahard, D Salgado, A Pathirana, R Velazquez, S McGuigan, C De Clercq, E Balzarini, J
Citation: D. Saboulard et al., Characterization of the activation pathway of phosphoramidate triester prodrugs of stavudine and zidovudine, MOLEC PHARM, 56(4), 1999, pp. 693-704

Authors: McGuigan, C Sutton, PW Cahard, D Turner, K O'Leary, G Wang, Y Gumbleton, M De Clercq, E Balzarini, J
Citation: C. Mcguigan et al., Synthesis, anti-human immunodeficiency virus activity and esterase lability of some novel carboxylic ester-modified phosphoramidate derivatives of stavudine (d4T), ANTIVIR CHE, 9(6), 1998, pp. 473-479

Authors: Cahard, D Duhamel, L Lecomte, S Poirier, JM
Citation: D. Cahard et al., Prenylation reaction performed with catalytically generated potassium prenal dienolate, SYNLETT, (12), 1998, pp. 1399-1401
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