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Synthesis of racemic 9-(6- and 2,6-substituted 9H-purin-9-yl)-5-oxatricyclo[4.2.1.03,7]nonane-3-methanols, novel conformationally locked carbocyclic nucleosides
- 1.0021558 - ÚOCHB 2006 RIV CZ eng J - Journal Article
Hřebabecký, Hubert - Masojídková, Milena - Holý, Antonín
Synthesis of racemic 9-(6- and 2,6-substituted 9H-purin-9-yl)-5-oxatricyclo[4.2.1.03,7]nonane-3-methanols, novel conformationally locked carbocyclic nucleosides.
[Syntéza racemických 9-(6- a 2,6-substituovaných 9H-purin-9-yl)-5-oxatricyklo[4.2.1.03,7]nonan-3-methanolů, nových konformačně uzamčených karbocyklických nukleosidů.]
Collection of Czechoslovak Chemical Communications. Roč. 70, č. 1 (2005), s. 103-123. ISSN 0010-0765
Institutional research plan: CEZ:AV0Z40550506
Keywords : amines * oximes * nucleosides
Subject RIV: CC - Organic Chemistry
Impact factor: 0.949, year: 2005
Novel racemic nucleoside analogues derived from 5-oxatricyclo[4.2.1.03,7]nonane-3-methanol were prepared. The compounds were tested for antiviral and cytotoxic activity.
Byla připravena nová racemická analoga nukleosidů odvozená od 5-oxatricyklo[4.2.1.03,7]nonan-3-methanolu. Látky byly testovány na protivirovou a cytotoxickou aktivitu.
Permanent Link: http://hdl.handle.net/11104/0110517
Number of the records: 1