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Results: 1-10 |
Results: 10
Synthesis and study of a new series of phosphoramidate derivatives as mononucleotide prodrugs
Authors: Egron, D Perigaud, C Gosselin, G Aubertin, AM Imbach, JL
Citation: D. Egron et al., Synthesis and study of a new series of phosphoramidate derivatives as mononucleotide prodrugs, NUCLEOS NUC, 20(4-7), 2001, pp. 751-754
Rational design of a new series of pronucleotide
Authors: Beltran, T Egron, D Pompon, A Lefebvre, I Perigaud, C Gosselin, G Aubertin, AM Imbach, JL
Citation: T. Beltran et al., Rational design of a new series of pronucleotide, BIOORG MED, 11(13), 2001, pp. 1775-1777
New bis(SATE) prodrug of AZT 5 '-monophosphate: In vitro anti-HIV activity, stability, and potential oral absorption
Authors: Shafiee, M Deferme, S Villard, AL Egron, D Gosselin, G Imbach, JL Lioux, T Pompon, A Varray, S Aubertin, AM Van den Mooter, G Kinget, R Perigaud, C Augustijns, P
Citation: M. Shafiee et al., New bis(SATE) prodrug of AZT 5 '-monophosphate: In vitro anti-HIV activity, stability, and potential oral absorption, J PHARM SCI, 90(4), 2001, pp. 448-463
Pharmacokinetics of bis(t-butyl-SATE)-AZTMP, a bispivaloylthioethyl prodrug for intracellular delivery of zidovudine monophosphate, in mice
Authors: Tan, XL Boudinot, FD Chu, CK Egron, D Perigaud, C Gosselin, G Imbach, JL
Citation: Xl. Tan et al., Pharmacokinetics of bis(t-butyl-SATE)-AZTMP, a bispivaloylthioethyl prodrug for intracellular delivery of zidovudine monophosphate, in mice, ANTIVIR CHE, 11(3), 2000, pp. 203-211
Radical cyclization of highly functionalized precursors: stereocontrol of ring closure of acyclic 1-substituted-2,4-dihydroxylated hex-5-enyl radicals
Authors: Roland, A Durand, T Egron, D Vidal, JP Rossi, JC
Citation: A. Roland et al., Radical cyclization of highly functionalized precursors: stereocontrol of ring closure of acyclic 1-substituted-2,4-dihydroxylated hex-5-enyl radicals, J CHEM S P1, (2), 2000, pp. 245-251
C-furanoside synthesis via intramolecular cyclization
Authors: Egron, D Durand, T Roland, A Vidal, JP Rossi, JC
Citation: D. Egron et al., C-furanoside synthesis via intramolecular cyclization, SYNLETT, (4), 1999, pp. 435-437
Anti-HIV pronucleotides: Sate versus phenyl as a protecting grow of AZT phosphoramidate derivatives
Authors: Beltran, T Egron, D Lefebvre, I Perigaud, C Pompon, A Gosselin, G Aubertin, AM Imbach, JL
Citation: T. Beltran et al., Anti-HIV pronucleotides: Sate versus phenyl as a protecting grow of AZT phosphoramidate derivatives, NUCLEOS NUC, 18(4-5), 1999, pp. 973-975
Synthesis and anti-HIV activity of some S-acyl-2-thioethyl (SATE) phosphoramidate derivatives of 3 '-azido-2 ',3 '-dideoxythymidine
Authors: Egron, D Perigaud, C Gosselin, G Aubertin, AM Imbach, JL
Citation: D. Egron et al., Synthesis and anti-HIV activity of some S-acyl-2-thioethyl (SATE) phosphoramidate derivatives of 3 '-azido-2 ',3 '-dideoxythymidine, NUCLEOS NUC, 18(4-5), 1999, pp. 981-982
Synthesis, anti-HIV activity and stability studies of 3 '-azido-2 ',3 '-dideoxythymidine 5 '-fluorophosphate
Authors: Egron, D Arzumanov, AA Dyatkina, NB Krayevsky, A Imbach, JL Aubertin, AM Gosselin, G Perigaud, C
Citation: D. Egron et al., Synthesis, anti-HIV activity and stability studies of 3 '-azido-2 ',3 '-dideoxythymidine 5 '-fluorophosphate, NUCLEOS NUC, 18(4-5), 1999, pp. 983-984
Synthesis of the tBuSATE pronucleotide of AZT by two different synthetic approaches
Authors: Lannuzel, M Egron, D Imbach, JL Gosselin, G Perigaud, C
Citation: M. Lannuzel et al., Synthesis of the tBuSATE pronucleotide of AZT by two different synthetic approaches, NUCLEOS NUC, 18(4-5), 1999, pp. 1001-1002
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