Abstract
5-(N-Hydroxy)carboxamidouridine (5) and 5-(N-hydroxy)carboxamido- methyluridine (6) have been synthesized; these hydroxamic acids incorporate a radical trap into a nucleoside structure, and are designed as potential inhibitors of ribonucleotide diphosphate reductase.
Original language | English |
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Pages (from-to) | 115-128 |
Number of pages | 14 |
Journal | Nucleosides and Nucleotides |
Volume | 16 |
Issue number | 1-2 |
Publication status | Published - 1997 |