Synthesis and antitumor activity of 1,2-dihydro-1-(2-deoxy-.beta.-D-erythro-pentofuranosyl)-2-oxo-5-methylpyrazine 4-oxide, a structural analog of thymidine
β Scribed by Bobek, M.; Bloch, A.; Berkowitz, P.; Bardos, T. J.
- Book ID
- 126831118
- Publisher
- American Chemical Society
- Year
- 1977
- Tongue
- English
- Weight
- 438 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0022-2623
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π SIMILAR VOLUMES
Synthesis and Antiviral Activities of 5-Substituted 1-(2-Deoxy-2-C-methylene-4-thio-Ξ²-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 Ξ²-anomers of these nucleosides po
(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