Nucleosides and nucleotides. 116. Convenient syntheses of 3-deazaadenosine, 3-deazaguanosine, and 3-deazainosine via ring closure of 5-ethynyl-1-β-D-ribofuranosylimidazole-4-carboxamide or -carbonitrile
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Perturbation of biochemical transmethylations by 3-deazaadenosine in vivo
2. 3-Deazaadenosine, an inhibitor of adenosylhomocysteine hydrolase, inhibits reproduction of rous sarcoma virus and transformation of chick embryo cells
3. Adenosylhomocysteine hydrolase inhibitors: Synthesis of 5′-deoxy-5′-(isobutylthio)-3-deazaadenosine and its effect on Rous sarcoma virus and Gross murine leukemia virus
4. Plasmodium falciparum: Antimalarial activity in culture of sinefungin and other methylation inhibitors
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1. Synthesis and biological activity of aza and deaza analogues of purine nucleosides;Russian Chemical Reviews;2021-12-01
2. Convenient Synthesis of 3‐Deazapurine Nucleosides (3‐Deazainosine, 3‐Deazaadenosine and 3‐Deazaguanosine) Using Inosine as a Starting Material;Current Protocols;2021-11
3. Access to 3-Deazaguanosine Building Blocks for RNA Solid-Phase Synthesis Involving Hartwig–Buchwald C–N Cross-Coupling;Organic Letters;2019-05-13
4. Synthesis of ethynylpyrene-modified 3-deaza-2′-deoxyguanosines as environmentally sensitive fluorescent nucleosides: Target DNA-sequence detection via changes in the fluorescence wavelength;Tetrahedron Letters;2019-03
5. The fluorescently responsive 3-(naphthalen-1-ylethynyl)-3-deaza-2′-deoxyguanosine discriminates cytidine via the DNA minor groove;Organic & Biomolecular Chemistry;2017
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