• Archives of Pharmacal Research
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• 제26권11호
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• pp.887-891
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• 2003

Novel trans-2,2-dimethylcyclopropyl nucleosides were synthesized as potential antiviral agents. The key intermediate, 3, was synthesized via five steps from ethyl chrysanthemate and condensed with purine bases using the Mitsunobu reaction to give six cyclopropyl nucleosides. These synthesized nucleosides did not show any significant antiviral activity against HSV-1, HSV-2, EMCV, Cox B3, or VSV, at concentrations up to 100 $\mu M$.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.356.1-356.1
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• 2002

The carbocyclic nucleosides have extensively studied as a promising antiviral agents having chemical and metabolical stability. In our research program for discovery of antiviral drugs. some novel dimethylcyclopropyl nucleosides possessing additional methyl spacer between purine bases and the ring was synthesized. The important intermediate, dimethylcyclopropyl alcohol was synthesized from ethyl chrysanthemate via its ozonolysis, isomerization reduction. (omitted)