Nucleosides. 121. Improved and general synthesis of 2'-deoxy-C-nucleosides. Synthesis of 5-(2-deoxy-.beta.-D-erythro-pentofuranosyl)uracil, -1-methyluracil, -1,3-dimethyluracil, and -isocytosine
โ Scribed by Pankiewicz, Krzysztof; Matsuda, Akira; Watanabe, Kyoichi A.
- Book ID
- 126980822
- Publisher
- American Chemical Society
- Year
- 1982
- Tongue
- English
- Weight
- 586 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-3263
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๐ SIMILAR VOLUMES
(2-Deoxy-D-erythro-pentofuranosyl)imidazole nucleosides have been synthesised by glycosylation of the sodium salt of ethyl 5-aminoimidazole-4-carboxylate with 2-deoxy-3,5-di-O-p-toluoyl-alpha-D-erythro-pentofuranosyl chloride. Glycosylation of ethyl 5-aminoimidazole-4-carboxylate with 2-deoxy-beta-D
Synthesis and Antiviral Activities of 5-Substituted 1-(2-Deoxy-2-C-methylene-4-thio-ฮฒ-D-erythro-pentofuranosyl) uracils. -A variety of the title nucleosides [cf. (VII)/(VIII), (X)] are prepared using sila-Pummerer-type glycosylation as key step. The majority of the ฮฒ-anomers of these nucleosides po