A lithiation route to c-5 substitution of an imidazole nucleoside and its application to the synthesis of 3-deazaguanosine
- 1 January 1986
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 42 (7), 1971-1980
- https://doi.org/10.1016/s0040-4020(01)87613-4
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- Synthesis and antiviral evaluation of nucleosides of 5-methylimidazole-4-carboxamideJournal of Medicinal Chemistry, 1985
- Synthesis of bredinin from 5-aminoimidazole-4-carboxamide-ribofuranoside (AICA-riboside).CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
- A simplified synthesis of 8-substituted purine nucleosides via lithiation of 6-chloro-9-(2,3-O-isopropylidene-.BETA.-D-ribofuranosyl)purine.CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
- “Umpulong” of reactivity at the C-6 position of uridine: a simple and general method for 6-substituted uridinesTetrahedron, 1982
- Synthesis and antiviral and antimicrobial activity of certain 1-.beta.-D-ribofuranosyl-4,5-disubstituted imidazolesJournal of Medicinal Chemistry, 1976
- Synthesis of 5-fluoro-1-β-D-ribofuranosylimidazole-4-carboxamide, an antiviral agent and inhibitor of polynucleotide biosynthesisTetrahedron Letters, 1975
- Nucleosides of 4-substituted imidazolesThe Journal of Organic Chemistry, 1975
- Fluoroimidazoles as antiviral agents and inhibitors of polynucleotide biosynthesisLife Sciences, 1975
- Studies on bredinin. III. Chemical synthesis of bredinin. (A novel imidazole nucleoside).CHEMICAL & PHARMACEUTICAL BULLETIN, 1975
- Imidazole Nucleosides and NucleotidesChemical Reviews, 1967