Synthesis and antiviral and cytostatic activities of carbocyclic nucleosides incorporating a modified cyclopentane ring. 1: Guanosine analogues

Article abstract of DOI:10.1080/07328319708002530

Six new carbocyclic nucleosides were prepared by constructing a guanine (compounds 6, 8 and 10) or 8-azaguanine (compounds 7, 9 and 11) base on the amino group of (1R, cis)-3-(aminomethyl)-1,2,2-trimethylcyclopentylmethanol (2), and their activities again

Full text of DOI:10.1080/07328319708002530

Nucleosides and Nucleotides
ISSN: 0732-8311 (Print) (Online) Journal homepage: http://www.tandfonline.com/loi/lncn19
Synthesis and Antiviral and Cytostatic Activities of
Carbocyclic Nucleosides Incorporating a Modified
Cyclopentane Ring. I: Guanosine Analogues
J. M. Blanco , O. Caamaño , F. Fernández , G. Gómez , M. I. Nieto , J. Balzarini ,
E. Padalko & E. De Clercq
To cite this article: J. M. Blanco , O. Caamaño , F. Fernández , G. Gómez , M. I. Nieto , J.
Balzarini , E. Padalko & E. De Clercq (1997) Synthesis and Antiviral and Cytostatic Activities of
Carbocyclic Nucleosides Incorporating a Modified Cyclopentane Ring. I: Guanosine Analogues,
Nucleosides and Nucleotides, 16:1-2, 159-171, DOI: 10.1080/07328319708002530
To link to this article: http://dx.doi.org/10.1080/07328319708002530
Published online: 20 Aug 2006.
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Date: 08 June 2016, At: 02:05