Synthesis of purine nucleoside analogues derived from carbocyclic 5-C-(hydroxymethyl)hexopyranoses

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F04%3A00100872" target="_blank" >RIV/61388963:_____/04:00100872 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Result language
angličtina
Original language name
Synthesis of purine nucleoside analogues derived from carbocyclic 5-C-(hydroxymethyl)hexopyranoses
Original language description
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
Czech name
Synthesa analog purinových nukleosidů odvozených od karbocyklických 5-C-(hydroxymethyl)hexopyranos
Czech description
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

Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Project
<a href="/en/project/GA203%2F02%2F0035" target="_blank" >GA203/02/0035: Nucleoside carba analogues containing substituted cyclohexanes: compounds with potential biological effects</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year
2004
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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