Synthests and Biological Evaluation of a Series of Substituted-2-Pyridine-C-Nucleosides. Part II
- 1 August 1986
- journal article
- research article
- Published by Taylor & Francis in Nucleosides, Nucleotides and Nucleic Acids
- Vol. 5 (4) , 441-455
- https://doi.org/10.1080/07328318608068685
Abstract
A cyclistation reaction of the D-allo- and D-altro isomers of 2-(2, 4:3, 5′-di-O-benzylidenepentitol-1-yl)pyridine derivatives to afford the corresponding substituted 2-(D-ribofuranosyl) pyridine-C-nucleosides, was investigated. The latter compounds were obtained in good yield (90%) if the reaction was performed in 1 N HCI. The structures were confirmed by 13C-NMR studies and an HPLC method with was developed specifically for a determination of their purity. All compounds were evaluated for biological activity in a variety of antiviral and antitumor cell systems in vitro.This publication has 8 references indexed in Scilit:
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