32
Views
24
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis and Biological Activity of Cyclohexenyl Nucleosides. cis-5-(9H-Purin-9-yl)-3-cyclohexenyl Carbinols and Their 8-Azapurinyl Analogs

&
Pages 2061-2077 | Received 03 Aug 1995, Accepted 13 Sep 1995, Published online: 24 Sep 2006
 

Abstract

5-Azido-3-cyclohexenecarboxylic acid was reduced to an aminocyclohexenyl-carbinol which was coupled with either 5-amino-4,6-dichloropyrimidine or 2-amino-4,6-dichloropyrimidine, giving 5-pyrimidinyl-3-cyclohexencarbinols. Condensation with triethylorthoformate or nitrous acid formed the purine and 8-azapurine ring systems, respectively. Anti-HIV-1 and cytotoxicity testing results are also described.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.