Issue 4, 1995

Synthesis of uridine derivatives containing strategically placed radical traps as potential inhibitors of ribonucleotide reductase

Abstract

A series of uridine derivatives have been prepared with a view to inhibiting the enzyme ribonucleotide reductase by trapping the radical responsible for initiating the reduction. These have an oxime ether on the beta face at C-3 or C-2 of the ribose moiety.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1995, 395-404

Synthesis of uridine derivatives containing strategically placed radical traps as potential inhibitors of ribonucleotide reductase

S. P. Auguste and D. W. Young, J. Chem. Soc., Perkin Trans. 1, 1995, 395 DOI: 10.1039/P19950000395

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements