Pyrazole related nucleosides 5. Synthesis and biological activity of 2'- deoxy-2',3'-dideoxy- and acyclo-analogues of 4-iodo-1-β-D-ribofuranosyl-3- carboxymethyl pyrazole (IPCAR)

Article abstract of DOI:10.1080/15257770008035019

Continuing our studies on the structure-activity relationships (SAR) of 4-iodo-1-β-D-ribofuranosyl-3-carboxymethyl pyrazole (IPCAR), the ribofuranosyl moiety has been substituted with acyclic chains, namely 1-[(2- hydroxyethoxy)methyl]- and 1-[(1,3-dihydr

Full text of DOI:10.1080/15257770008035019

Nucleosides, Nucleotides and Nucleic Acids
ISSN: 1525-7770 (Print) 1532-2335 (Online) Journal homepage: http://www.tandfonline.com/loi/lncn20
Pyrazole Related Nucleosides 5.1 Synthesis and
Biological Activity of 2′-Deoxy- 2′, 3′-dideoxy- and
Acyclo-analogues of 4-Iodo-1-β-D-ribofuranosyl-3-
carboxymethyl Pyrazole (IPCAR)
Stefano Manfredini , Pier Giovanni Baraldi , Rita Bazzanini , Elisa Durini ,
Silvia Vertuani , Alessandra Pani , Tiziana Marceddu , Francesca Demontis ,
Laura Vargiu & Paolo La Colla
To cite this article: Stefano Manfredini , Pier Giovanni Baraldi , Rita Bazzanini , Elisa
Durini , Silvia Vertuani , Alessandra Pani , Tiziana Marceddu , Francesca Demontis , Laura
Vargiu & Paolo La Colla (2000) Pyrazole Related Nucleosides 5.1 Synthesis and Biological
Activity of 2′-Deoxy- 2′, 3′-dideoxy- and Acyclo-analogues of 4-Iodo-1-β-D-ribofuranosyl-3-
carboxymethyl Pyrazole (IPCAR), Nucleosides, Nucleotides and Nucleic Acids, 19:4, 705-722,
DOI: 10.1080/15257770008035019
To link to this article: http://dx.doi.org/10.1080/15257770008035019
Published online: 24 Sep 2006.
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Date: 05 November 2015, At: 23:57