Issue 8, 1999

The synthesis of novel 3′,5′-homocyclic nucleotides as potential anti-HIV agents

Abstract

(5S )-(5-tert-Butyldimethylsiloxymethyl)furan-2(5H )-one has been converted into cytosine 2′,3′-dideoxy-3′,5′-homocyclic monophosphate (and its 5-fluoro congener) together with an adenosine homocyclic monophosphate. These were designed as inhibitors of HIV reverse transcriptase although they did not possess such activity.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1999, 969-978

The synthesis of novel 3′,5′-homocyclic nucleotides as potential anti-HIV agents

M. G. B. Drew, S. Gorsuch, J. H. M. Gould and J. Mann, J. Chem. Soc., Perkin Trans. 1, 1999, 969 DOI: 10.1039/A900800D

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