Tautomerism in cytidine

descriptionPublicationkeyboard_double_arrow_right Article 01 May 1971 English Publisher:WileyJournal:Biopolymers, volume 10, pages 923-933 (issn: 0006-3525, eissn: 1097-0282,

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Authors: W C, Johnson; P M, Vipond; J C, Girod;

doi: 10.1002/bip.360100514

pmid: 5572634

Tautomerism in cytidine

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Abstract

AbstractThe large change in the electronic absorption spectrum of cytidine on going from an aqueous to an aprotic medium is attributed to the existence of a hydrogen bonded solvent‐solute complex in solvents capable of donating a proton. The spectrum of cytidine in a variety of solvents and the spectra of a number of nontautomerising model compounds are presented. The tautomerisin of cytidine and its biological implications are discussed.

Related Organizations

Oregon State University
United States

Keywords

Solutions, Isomerism, Spectrum Analysis, Nucleosides

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