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Synthesis of novel 3 '-deoxy-3 '-C-hydroxymethyl nucleosides with conformationally rigid sugar moiety as potential antiviral agents
- Synthesis of novel 3 '-deoxy-3 '-C-hydroxymethyl nucleosides with conformationally rigid sugar moiety as potential antiviral agents
- Chun, MW; Kim, MJ; Jo, UH; Kim, JH; Kim, HD; Jeong, LS
- Ewha Authors
- SCOPUS Author ID
- Issue Date
- Journal Title
- NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS
- NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS vol. 20, no. 4-7, pp. 699 - 702
- MARCEL DEKKER INC
- SCIE; SCOPUS
- Document Type
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- Based on the fact that the ring expanded 3'-C-hydroxymethyl analogue of oxetanocin A exhibited potent antiviral activity, two types of conformationally rigid 3'-C-hydroxymethyl derivatives in which 2'-hydroxyl group is linked to the 4'-position or to the 6'-position were synthesized starting from 1,2;5,6-di-O-isopropylidene-D-glucose, respectively.
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