2′-C-alkylribonucleosides: Design, synthesis, and conformation

Article abstract of DOI:10.1080/07328319708006205

Certain 2′-C-alkylribonucleotides have been designed as potential mechanism-based inactivators of ribonucleotide reductases. A short, flexible route toward the corresponding nucleosides and NMR evidence concerning their preferred solution conformations are discussed. Copyright

Full text of DOI:10.1080/07328319708006205

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Nucleosides and Nucleotides
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2′-C-Alkylribonucleosides: Design,
Synthesis, and Conformation
Rogers E. Harry-O'kuru a , Emily A. Kryjak a & Michael S. Wolfe a
a Department of Pharmaceutical Sciences , University of
Tennessee , Room 327, 847 Monroe St., Memphis, TN, 38163
Published online: 16 Aug 2006.
To cite this article: Rogers E. Harry-O'kuru , Emily A. Kryjak & Michael S. Wolfe (1997) 2′-C-
Alkylribonucleosides: Design, Synthesis, and Conformation, Nucleosides and Nucleotides, 16:7-9,
1457-1460, DOI: 10.1080/07328319708006205
To link to this article: http://dx.doi.org/10.1080/07328319708006205
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