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Bioorg Khim ; 12(6): 819-27, 1986 Jun.
Artigo em Russo | MEDLINE | ID: mdl-3778532

RESUMO

A number of ribavirin analogues were prepared in which the ribose moiety was replaced with acyclic substituents imitating some fragments of the ribose ring: 2,3-dihydroxy-prop-1-yl, 3-hydroxymethyl-4-hydroxy-2-oxabut-1-yl, 4,5-dihydroxy-2-oxapent-1-yl and 1,5-dihydroxy-3-oxapent-2-yl. These analogues were synthesized by direct alkylation of ethyl 1,2,4-triazole-3-carboxylate with suitable agents followed by ammonolysis. New convenient methods for preparing the alkylating agents were developed.


Assuntos
Ribavirina/síntese química , Ribonucleosídeos/síntese química , Fenômenos Químicos , Química , Ribavirina/análogos & derivados
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