2,6-Diazidopurine Deoxyribo-Nucleoside as Substrate for the Click Reaction

Abstracts of Riga Technical University 55th International Scientific Conference : Section: Material Science and Applied Chemistry 2014
Dace Cīrule, Kristers Ozols, Ērika Bizdēna, Irina Novosjolova

The chemistry of triazolyl-substituted purine nucleosides is attractive since some of them exhibit antiviral, anticancer or fluorescent properties. Our group has reported the synthesis of 2,6-bistriazolyl purine arabino- and ribo-nucleosides using Cu(I) catalysed azide - alkyne 1,3-dipolar cycloaddition reaction. Various nucleophilic substitution reactions with the obtained products were carried out. In addition to our previous work, herein we report the synthesis of the novel bis-triazolyl purine deoxyribo-nucleosides and their reactions with N- nucleophiles.

Keywords
Deoxyribonucleosides, "Click" chemistry

Cīrule, D., Ozols, K., Bizdēna, Ē., Novosjolova, I. 2,6-Diazidopurine Deoxyribo-Nucleoside as Substrate for the Click Reaction. In: Abstracts of Riga Technical University 55th International Scientific Conference : Section: Material Science and Applied Chemistry, Latvia, Rīga, 14-17 October, 2014. Rīga: 2014, pp.19-19.

Publication language
English (en)