Synthesis and anti-HCMV activity of novel cyclopropyl phosphonic acid nucleosides
Aihong Kim1, Joon Hee Hong, Chang Hyun Oh
1College of Pharmacy, Chosun University, Kwangju, Republic of Korea.
Nucleosides, Nucleotides & Nucleic Acids
|October 28, 2006
Abstract:
A simple synthetic route for novel acyclic phosphonate nucleosides is described. The characteristic cyclopropyl moiety 8 was constructed employing the Simmons-Smith reaction as key step starting from simple acyclic 2-butene-1,4-diol. The condensation of the mesylate 11 with natural nucleosidic bases (A,C,T,U) under nucleophilic substitution conditions (K2CO3, 18-Crown-6, DMF) and hydrolysis afforded the target nucleosides 16, 17, 18, and 19. In addition, the antiviral evaluations against various viruses were performed.
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