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Mini Reviews in Medicinal Chemistry|May 12, 2004
"Lock-in"-cycloSal-pronucleotides - a new generation of chemical Trojan Horses?Chris Meier, Manuel F H Ruppel, Dalibor Vukadinovic, et al.Chemmedchem|October 22, 2020
γ-Non-Symmetrically Dimasked TriPPPro Prodrugs as Potential Antiviral Agents against HIVChenglong Zhao, Xiao Jia, Dominique Schols, et al.Bioorganic & Medicinal Chemistry|December 3, 2014
Synthesis and analysis of potential α1,3-fucosyltransferase inhibitorsKatrin Seelhorst, Tomas Piernitzki, Nathalie Lunau, et al.Chemmedchem|April 8, 2015
Bis(benzoyloxybenzyl)-DiPPro nucleoside diphosphates of anti-HIV active nucleoside analoguesLina Weinschenk, Tristan Gollnest, Dominique Schols, et al.Obstetrics and Gynecology|June 12, 2003
The implications of a false positive second-trimester serum screen for Down syndromeAnne M Summers, Tianhua Huang, Chris Meier, et al.Journal of Medicinal Chemistry|May 14, 2004
Interaction of cycloSal-pronucleotides with cholinesterases from different origins. A structure-activity relationshipChris Meier, Christian Ducho, Ulf Görbig, et al.Nucleosides, Nucleotides & Nucleic Acids|March 27, 2004
Second generation of cycloSal-pronucleotides with esterase-cleavable sites: the "lock-in"-conceptChris Meier, Manuel F H Ruppel, Dalibor Vukadinović, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|July 26, 2012
Stereoselective synthesis of D- and L-carbocyclic nucleosides by enzymatically catalyzed kinetic resolutionMiriam Mahler, Bastian Reichardt, Philip Hartjen, et al.Antiviral Research|April 6, 2019
Cell line-dependent activation and antiviral activity of T-1105, the non-fluorinated analogue of T-705 (favipiravir)Johanna Huchting, Evelien Vanderlinden, Ria Van Berwaer, et al.International Journal of Antimicrobial Agents|April 20, 2006
Antiviral activity of cyclosaligenyl prodrugs of the nucleoside analogue bromovinyldeoxyuridine against herpes virusesAstrid Meerbach, Chris Meier, Andreas Sauerbrei, et al.Pageof 14