Resolution of enantiomers of uridine analogs, potential antiviral agents
- 1 November 1996
- journal article
- Published by Elsevier in Journal of Chromatography A
- Vol. 752 (1-2) , 131-146
- https://doi.org/10.1016/s0021-9673(96)00507-9
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Conformationally Locked Nucleoside Analogs. Synthesis of Dideoxycarbocyclic Nucleoside Analogs Structurally Related to Neplanocin CJournal of Medicinal Chemistry, 1994
- Asymmetric synthesis and biological evaluation of .beta.-L-(2R,5S)- and .alpha.-L-(2R,5R)-1,3-oxathiolane-pyrimidine and -purine nucleosides as potential anti-HIV agentsJournal of Medicinal Chemistry, 1993
- Synthesis and antiviral activity of methyl derivatives of 9-[2-(phosphonomethoxy)ethyl]guanineJournal of Medicinal Chemistry, 1992
- Activities of the four optical isomers of 2',3'-dideoxy-3'-thiacytidine (BCH-189) against human immunodeficiency virus type 1 in human lymphocytesAntimicrobial Agents and Chemotherapy, 1992
- The Controlled Stereospecific Reduction of Cyclopentenyl Cytosine (CPE-C) to Carbodine and IsocarbodineNucleosides and Nucleotides, 1992
- Preparative separation and analysis of the enantiomers of [3H]Abbott-69992, an HIV anti-infective nucleoside, by ligand-exchange high-performance liquid chromatographyJournal of Chromatography A, 1991
- Carbovir: the (—) enantiomer is a potent and selective antiviral agent against human immunodeficiency virus in vitroAntiviral Research, 1991
- The effect of alcoholic mobile phase modifiers on retention and stereoselectivity on a commercially available cellulose-based HPLC chiral stationary phase: An unexpected reversal in enantiometric elution orderChromatographia, 1989
- Resolution of enantiomeric amides on a cellulose tribenzoate chiral stationary phaseJournal of Chromatography A, 1987
- Carbocyclic nucleosidesMedicinal Research Reviews, 1986