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Conjugates of 1,2,3-triazoles and acyclic pyrimidine nucleoside analogues: syntheses and X-ray crystallographic studies (CROSBI ID 192218)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Korunda, Silvija ; Krištafor, Svjetlana ; Cetina, Mario ; Raić-Malić, Silvana Conjugates of 1,2,3-triazoles and acyclic pyrimidine nucleoside analogues: syntheses and X-ray crystallographic studies // Current organic chemistry, 17 (2013), 10; 1114-1124. doi: 10.2174/1385272811317100012

Podaci o odgovornosti

Korunda, Silvija ; Krištafor, Svjetlana ; Cetina, Mario ; Raić-Malić, Silvana

engleski

Conjugates of 1,2,3-triazoles and acyclic pyrimidine nucleoside analogues: syntheses and X-ray crystallographic studies

The synthesis of novel acyclic pyrimidine nucleoside analogues with 1, 2, 3-triazole ring bound via ethylene spacer or directly to C-5 of pyrimidine ring has been reported. 1, 4- Disubstituted 1, 2, 3-triazoles were synthesized by click chemistry approach using regioselective copper(I)-catalyzed 1, 3-dipolar cycloaddition reaction between terminal alkyne and azido pyrimidines under both conventional (method A) and microwave (method B) conditions. N-Alkylation of triazolyl pyrimidines afforded 5-[2-(1, 2, 3- triazolyl)ethyl]pyrimidine derivatives with penciclovir-, ganciclovir-like and 2, 3- dihydroxypropyl side chain, as well as 5-(1, 2, 3- triazolyl)pyrimidine derivatives with penciclovir- and ganciclovir-like side chain. The stereostructures of 2-hydroxyethyl, 2- tosyloxyethyl, 2-azidoethyl and 4-acetoxymethyl- 1, 2, 3-triazolyl C-5 substituted pyrimidine derivatives were unambiguously confirmed by their X-ray crystal structure analysis.

acyclic pyrimidine nucleoside ; azide-alkyne cycloaddition ; click chemistry ; 1, 4-disubstituted 1, 2, 3-triazoles ; X-ray diffraction ; supramolecular assembling

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Podaci o izdanju

17 (10)

2013.

1114-1124

objavljeno

1385-2728

1875-5348

10.2174/1385272811317100012

Povezanost rada

Kemija

Poveznice
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