A novel cyclization reaction of a C-6 substituted uridine analog: An entry to 5,6-dialkylated uridine derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Targets for the Antiviral Activity of Pyrimidine and Purine Nucleoside Analogues
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4. Synthesis and biological evaluation of 6-ethynyluracil, a thiol-specific alkylating pyrimidine
5. Antiviral activity of certain substituted purine and pyrimidine nucleosides
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. References;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
2. A chemical model for the fragmentation reaction in thymidylate synthase catalysis. Synthesis and evaluation of a 5-methylene-1-(1,2,3,4-tetrahydroquinolyl)-6-allyluridine;The Journal of Organic Chemistry;1993-05
3. Lithiation Chemistry of Uridine Derivatives: Access to a New Anti-HIV-1 Lead;Nucleosides and Nucleotides as Antitumor and Antiviral Agents;1993
4. From Lithiation Studies of Nucleosides to the Finding of a New Lead for Anti-HIV-1 Agents.;Journal of Synthetic Organic Chemistry, Japan;1991
5. ChemInform Abstract: A Novel Cyclization Reaction of a C-6 Substituted Uridine Analog: An Entry to 5,6-Dialkylated Uridine Derivatives.;ChemInform;1990-07-24
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