Novel spaeered cyclopropane nucleoside analogues possessing both a hydroxyethyl group and an additional methylene spacer between the base and the ring were synthesized starting from 3-buten-l-ol. After tetrahydropyranylation, eyelopropanation, and reduction the target molecules were obtained by Mits
Synthesis of fluorinated analogues of acyclic nucleosides as potential antiviral agents
โ Scribed by Pierfrancesco Bravo; Giuseppe Resnati; Fiorenza Viani
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 40 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-1139
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