Abstract
On the basis of potent anti-hepatitis C virus (HCV) activity of 2'-C-hydroxymethyladenosine, 3'-C-hydroxymethyl-substituted pyrimidine and purine nucleosides as potential anti-HCV agents were designed and synthesized from D-xylose via stereoselective Grignard reaction and conversion of the vinyl into hydroxymethyl group as key steps.
| Original language | English |
|---|---|
| Pages (from-to) | 843-849 |
| Number of pages | 7 |
| Journal | Archives of Pharmacal Research |
| Volume | 31 |
| Issue number | 7 |
| DOIs | |
| State | Published - Jul 2008 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- 3'-C-hydroxymethyl nucleosides
- Anti-hepatitis C virus (HCV) activity
- Neighboring group effect
- Stereoselective Grignard reaction
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