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Journal of Medicinal Chemistry|May 19, 2020
Anti-HIV-Active Nucleoside Triphosphate ProdrugsXiao Jia, Dominique Schols, Chris MeierChemmedchem|March 12, 2014
The DiPPro approach: synthesis, hydrolysis, and antiviral activity of lipophilic d4T diphosphate prodrugsTilmann Schulz, Jan Balzarini, Chris MeierJournal of Medicinal Chemistry|August 30, 2023
Pronucleotides of 2',3'-Dideoxy-2',3'-Didehydrothymidine as Potent Anti-HIV CompoundsXiao Jia, Dominique Schols, Chris MeierJournal of Medicinal Chemistry|March 6, 2007
Enzymatically activated cycloSal-d4T-monophosphates: The third generation of cycloSal-pronucleotidesNicolas Gisch, Jan Balzarini, Chris MeierThe Journal of Organic Chemistry|December 16, 2006
Synthesis and properties of oligonucleotides containing C8-deoxyguanosine arylamine adducts of borderline carcinogensNicolas Böge, Sonja Gräsl, Chris MeierChemmedchem|September 12, 2014
Nucleoside mono- and diphosphate prodrugs of 2',3'-dideoxyuridine and 2',3'-dideoxy-2',3'-didehydrouridineFlorian Pertenbreiter, Jan Balzarini, Chris MeierJournal of Medicinal Chemistry|October 16, 2010
Diastereoselective synthesis of aryloxy phosphoramidate prodrugs of 3'-deoxy-2',3'-didehydrothymidine monophosphateCristina Arbelo Roman, Jan Balzarini, Chris MeierNucleosides, Nucleotides & Nucleic Acids|December 11, 2007
New developments of the "lock-in" modified cycloSal-d4TMPsDalibor Vukadinović-Tenter, Jan Balzarini, Chris MeierJournal of Medicinal Chemistry|October 2, 2008
Intracellular trapping of cycloSal-pronucleotides: modification of prodrugs with amino acid estersHenning J Jessen, Jan Balzarini, Chris MeierJournal of Medicinal Chemistry|November 1, 2002
CycloSal-BVDUMP pronucleotides: how to convert an antiviral-inactive nucleoside analogue into a bioactive compound against EBVChris Meier, Andreas Lomp, Astrid Meerbach, et al.Pageof 14