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Synthesis of purine nucleoside analogues derived from carbocyclic 5-C-(hydroxymethyl)hexopyranoses
- 1.0100872 - UOCHB-X 20043060 RIV CZ eng J - Journal Article
Hřebabecký, Hubert - Masojídková, Milena - Holý, Antonín
Synthesis of purine nucleoside analogues derived from carbocyclic 5-C-(hydroxymethyl)hexopyranoses.
[Synthesa analog purinových nukleosidů odvozených od karbocyklických 5-C-(hydroxymethyl)hexopyranos.]
Collection of Czechoslovak Chemical Communications. Roč. 69, č. 2 (2004), s. 435-452. ISSN 0010-0765
R&D Projects: GA ČR GA203/02/0035
Institutional research plan: CEZ:AV0Z4055905
Keywords : nucleosides * purines * adenine
Subject RIV: CC - Organic Chemistry
Impact factor: 1.062, year: 2004
New nucleoside analogues of adenine, 6-(cyclopropylamino)purine, and guanine were prepared from amino derivatives of 5a-carba-5-C-(hydroxymethyl)-alpha-D-idopyranose and 5a-carba-5-C-(hydroxymethyl)-beta-D-gulopyranose
Nová nukleosidová analoga adeninu, 6-(cyklopropylamino)purinu a guaninu byla připravena z aminoderivátů 5a-karba-5-C-(hydroxymethyl)-alfa-D-idopyranosy a karba-5-C-(hydroxymethyl)-beta-D-gulopyranosy
Permanent Link: http://hdl.handle.net/11104/0008356
Number of the records: 1