Scientific article
English

3′-Deoxy-3′-Hydroxyamino-β-D-Xylofuranosyluracil and Derivatives Thereof

Published inNucleosides & Nucleotides, vol. 7, no. 2, p. 249-269
Publication date1988
Abstract

The title compound was prepared by reduction of the oxime of the 3′-ketouridine. Condensation with aldehydes gave a series of nitrones whose reduction afforded “second generation” hydroxylamines, some of which showing antiviral activity. The nitroxide free radicals formed upon oxidation of hydroxylamines gave good ESR spectra useful for configurational and conformational assignments.

Citation (ISO format)
TRONCHET, Jean Marcel Julien et al. 3′-Deoxy-3′-Hydroxyamino-β-D-Xylofuranosyluracil and Derivatives Thereof. In: Nucleosides & Nucleotides, 1988, vol. 7, n° 2, p. 249–269. doi: 10.1080/07328318808070208
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ISSN of the journal0732-8311
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