J-L. Imbach

Synthesis and Antiviral Evaluation of SATE-Foscarnet Prodrugs and New Foscarnet—AZT Conjugates

Chris Meier, A.M. Aubertin, M. De Monte et al. · Antiviral chemistry & chemotherapy · 1998 · 22 citations

Pharmacy, Medicinal Chemistry, Pharmacology +17

Human Immunodeficiency Virus Resistance to AZT in MOLT4/8 Cells is Associated with a Lack of AZT Phosphorylation and is Bypassed by AZT-Monophosphate SATE Prodrugs

Jindřich Činátl, Bettina Gröschel, Richard Zehner et al. · Antiviral chemistry & chemotherapy · 1997 · 18 citations

Life Sciences, Infectious Diseases, Cellular Immunology +13

Antiviral Activity and Intracellular Metabolism of Bis(tButylSATE) Phosphotriester of β-L-2′,3'Dideoxyadenosine, a Potent Inhibitor of HIV and HBV Replication

L Placidi, Achraf Al Faraj, AG Loi et al. · Antiviral chemistry & chemotherapy · 2001 · 14 citations

Life Sciences, Biochemistry, Molecular Biology +17

The conformational analysis of heterocyclic systems. Part VIII. Kinetics of quaternisation of N-alkylpiperidines and N-alkylpiperazines in acetonitrile

J-L. Imbach, Alan R. Katritzky, R. A. KOLINSKI · Journal of the Chemical Society B Physical Organic · 1966 · 13 citations

Natural Sciences, Chemistry, Medicinal Chemistry +10

Anti-HIV Pronucleotides: SATE Versus Phenyl as a Protecting Group of AZT Phosphoramidate Derivatives

Thierry Beltran, David Egron, Isabelle Lefèbvre et al. · Nucleosides and Nucleotides · 1999 · 12 citations

Pharmacy, Medicinal Chemistry, Pharmacokinetics +13