Abstract
Novel 2′-C-methyl-cyclopropyl-fused carbocyclic nucleosides as potential anti-HCV agents were stereoselectively synthesized, utilizing regioselective cleavage of the isopropylidene group and cyclic sulfate chemistry as key steps.
| Original language | English |
|---|---|
| Pages (from-to) | 1021-1024 |
| Number of pages | 4 |
| Journal | Nucleosides, Nucleotides and Nucleic Acids |
| Volume | 26 |
| Issue number | 8-9 |
| DOIs | |
| State | Published - Aug 2007 |
Bibliographical note
Funding Information:This research was supported by a grant from the Korea Research Foundation (KRF-2005-005-J01502). Anti-HCV assay by Gilead Sciences is greatly appreciated. Address correspondence to Lak Shin Jeong, College of Pharmacy, Ewha Womans University, Seoul 120 750, Korea. E-mail: [email protected]
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
- Anti-HCV agents
- Cyclic sulfate chemistry
- Hepatitis C virus
- Regioselective opening
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