Synthesis and biological activity of cyclohexenyl nucleosides. cis-5-(9H- purin-9-yl)-3-cyclohexenyl carbinols and their 8-azapurinyl analogs

Article abstract of DOI:10.1080/15257779508010724

5-Azido-3-cyclohexenecarboxylic acid was reduced to an aminocyclohexenylcarbinol which was coupled with either 5-amino-4,6- dichloropyrimidine or 2-amino-4,6-dichloropyrimidine, giving 5-pyrimidinyl- 3-cyclohexencarbinols. Condensation with triethylorthof

Full text of DOI:10.1080/15257779508010724

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Nucleosides and Nucleotides
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Synthesis and Biological Activity of
Cyclohexenyl Nucleosides. cis-5-(9H-
Purin-9-yl)-3-cyclohexenyl Carbinols
and Their 8-Azapurinyl Analogs
Michael J. Konkel a & Robert Vince a
a Department of Medicinal Chemistry , College of Pharmacy
University of Minnesota , 308 Harvard Street, S.E., Minneapolis,
MN, 55455-0343
Published online: 24 Sep 2006.
To cite this article: Michael J. Konkel & Robert Vince (1995) Synthesis and Biological Activity of
Cyclohexenyl Nucleosides. cis-5-(9H-Purin-9-yl)-3-cyclohexenyl Carbinols and Their 8-Azapurinyl
Analogs, Nucleosides and Nucleotides, 14:9-10, 2061-2077, DOI: 10.1080/15257779508010724
To link to this article: http://dx.doi.org/10.1080/15257779508010724
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