Synthesis of 2-alkyl-3-hydroxy-4-pyridinone-ribonucleosides, potential oral iron chelators

Article abstract of DOI:10.1080/15257779508010712

Several ribonucleosides, named 2-alkyl-3-hydroxy-1-(β-D-ribofuranosyl or pyranosyl)-4-pyridinones, were synthesized in good yield. The method provides a useful means to obtain α-ketohydroxypyridin derivatives with different sugar moieties that, if used as

Full text of DOI:10.1080/15257779508010712

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Nucleosides and Nucleotides
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Synthesis of 2-Alkyl-3-hydroxy-4-
pyridinone-ribonucleosides, Potential
Oral Iron Chelators
Gang Liu a , Fred W. Bruenger a , Amy M. Barrios a & Scott C.
Miller a
a Division of Radiobiology, School of Medicine, University of
Utah, Bldg 585, Salt Lake City, UT, 84112, U.S.A.
Published online: 24 Sep 2006.
To cite this article: Gang Liu , Fred W. Bruenger , Amy M. Barrios & Scott C. Miller (1995)
Synthesis of 2-Alkyl-3-hydroxy-4-pyridinone-ribonucleosides, Potential Oral Iron Chelators,
Nucleosides and Nucleotides, 14:9-10, 1901-1904, DOI: 10.1080/15257779508010712
To link to this article: http://dx.doi.org/10.1080/15257779508010712
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