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A New Facile Synthesis and Antiviral Activity of Oxazofurin
- Source :
- Nucleosides and Nucleotides; March 1993, Vol. 12 Issue: 3 p359-368, 10p
- Publication Year :
- 1993
-
Abstract
- A new, more facile synthesis of oxazofurin, a structural analogue of tiazofurin, selenazofurin and ribavirin, has been carried out by rhodium catalyzed reaction of ethyl α-formyl-diazoacetate with 2,3, 5-tri-O-benzoyl-β-D-ribofu-ranosyl cyanide. When evaluated against DNA and RNA viruses, HIV-1 inclu-ded, oxazofurin was found inactive. It was also ineffective in potentiating the anti-HIV activity of 2', 3'-dideoxyadenosine.
Details
- Language :
- English
- ISSN :
- 07328311
- Volume :
- 12
- Issue :
- 3
- Database :
- Supplemental Index
- Journal :
- Nucleosides and Nucleotides
- Publication Type :
- Periodical
- Accession number :
- ejs11423626
- Full Text :
- https://doi.org/10.1080/07328319308017832