Proceedings of the PSK Conference (대한약학회:학술대회논문집)
- 2002.10a
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- Pages.366.2-366.2
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- 2002
SYNTHESIS OF [1-FLUORO-2.2-BIS-(HYDROXYMETHYL) CYCLOPROPYLMETHYL] PURINES AS ANTIVIRAL AGENTS
- Park, Ju-Hyun (Sookmyung Women′s University:) ;
- Choi, Myung-Hee (KRIC) ;
- Kim, Hee-Doo (KRIC) ;
- Lee, Chong-Kyo (KRICT)
- Published : 2002.10.01
Abstract
In an effort to search for the chemically and enzymatically stable carbonucleoside. we designed [1'-fluoro-2', 2'-bis-(hydroxymethyl) cyclopropyl methyl] purines. The underlying concept for our design is to seek relatively conformationally-locked compound with minimal structural disturbance from acyclic carbonucleoside such as acyclovir or penciclovir. To meet such a requirement. we need to introduce cyclopropane and fluorine moiety. (omitted)
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