Synthesis of 6-substituted uridines. synthesis of (R or S)-6-(3-amino-2-carboxypropyl)uridine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
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Cited by 12 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. An Intramolecular Anionic Migration of a Stannyl Group from the 6-Position of 1-(2-Deoxy- d - erythro -pent-1-enofuranosyl)uracil to the 2′-Position: Synthesis of 2′-Substituted 1′,2′-Unsaturated Uridines;Tetrahedron;2000-07
2. HEPT: From an investigation of lithiation of nucleosides towards a rational design of non-nucleoside reverse transcriptase inhibitors of HIV-1;Advances in Antiviral Drug Design;1999
3. Synthesis of 5-Arylthiouridines via Electrophilic Substitution of 5-Bromouridines with Diaryl Disulfides;Nucleosides, Nucleotides and Nucleic Acids;1998-01-01
4. A new class of nucleosides possessing unusual physical properties: syntheses, hydration, and structural equilibria of 1-(.beta.-D-glycofuranosyl)uracil-6-carboxaldehydes;The Journal of Organic Chemistry;1993-07
5. Lithiation Chemistry of Uridine Derivatives: Access to a New Anti-HIV-1 Lead;Nucleosides and Nucleotides as Antitumor and Antiviral Agents;1993
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