Synthesis of cyclonucleosides having a C–C bridge
Authors:
- 1 August 2008
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 64 (32) , 7453-7475
Abstract
No abstract availableKeywords
This publication has 67 references indexed in Scilit:
- Antiviral drugs in current clinical useJournal of Clinical Virology, 2004
- Antitumor activity of sugar‐modified cytosine nucleosidesCancer Science, 2004
- Experimental and Structural Evidence that Herpes 1 Kinase and Cellular DNA Polymerase(s) Discriminate on the Basis of Sugar PuckerJournal of the American Chemical Society, 2003
- Synthesis and Biological Evaluation of 5-Substituted Derivatives of the Potent Antiherpes Agent (north)-MethanocarbathymineJournal of Medicinal Chemistry, 2003
- Recent Advances in the Synthesis of Conformationally Locked Nucleosides and Their Success in Probing the Critical Question of Conformational Preferences by Their Biological TargetsNucleosides, Nucleotides & Nucleic Acids, 2003
- A Conformationally Locked Analogue of the Anti-HIV Agent Stavudine. An Important Correlation between Pseudorotation and Maximum AmplitudeJournal of Medicinal Chemistry, 2003
- Synthesis of a Bicyclic Analogue of AZT Restricted in an Unusual O4‘-Endo ConformationThe Journal of Organic Chemistry, 2001
- How do the gauche and anomeric effects drive the pseudorotational equilibrium of the pentofuranose moiety of nucleosides?Journal of the American Chemical Society, 1993
- Conformational analysis of the sugar ring in nucleosides and nucleotides. Improved method for the interpretation of proton magnetic resonance coupling constantsJournal of the American Chemical Society, 1973
- Conformational analysis of the sugar ring in nucleosides and nucleotides. New description using the concept of pseudorotationJournal of the American Chemical Society, 1972