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Synthesis of novel 1,3‐dioxolane nucleoside analogues
Author(s) -
Cai DongMei,
Lin KunHua,
Li MirtgZong,
Wen JiWu,
Li HongYan,
You TianPa
Publication year - 2004
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.20040221210
Subject(s) - chemistry , dioxolane , hydroxymethyl , nucleoside , thiazole , stereochemistry , nucleoside analogue , proton nmr , benzimidazole , organic chemistry
Novel 1,3‐dioxolane C‐nucleoside analogues of tiazofurin 2‐(2‐hydroxymethyl‐1,3‐dioxolan‐4‐yl)‐l,3‐thiazole‐4‐carboxamide as well as N ‐nucleoside analogues of substituted imidazoles 1‐(2‐hydroxymethyl‐1,3‐dioxolan‐4‐yl)‐4‐nitroimidazole and 1‐(2‐hydroxymethyl‐1,3‐dioxolan‐4‐yl)‐4,5‐dicyanoimidazole were synthesized from methyl acrylate through a multistep procedure. Their structures were confirmed by IR, 1 H NMR, 13 C NMR spectra and elemental analysis.