Synthesis of N4-amino and N4-hydroxy derivatives of 5-azacytidine. A facile rearrangement of the N4-amino derivative to 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazole
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F04%3A00100877" target="_blank" >RIV/61388963:_____/04:00100877 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Synthesis of N4-amino and N4-hydroxy derivatives of 5-azacytidine. A facile rearrangement of the N4-amino derivative to 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazole
Original language description
N4-Amino and N4-Hydroxy derivatives of the nucleoside antibiotic 5-azacytidine have been prepared. A facile rearrangement of the N4-amino derivative to 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazole and its mechanism was described
Czech name
Syntéza N4-amino a N4-hydroxyderivátů 5-azacytidinu. Snadný přesmyk N4-aminoderivátu na 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazol
Czech description
Byly připaveny N4-amino- a N4-hydroxyderiváty nukleosidového antibiotika 5-azacytidinu. Byl popsán snadný přesmyk tohoto N4-aminoderivátu na 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazol a jeho mechanismus
Classification
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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Result continuities
Project
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Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2004
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Collection of Czechoslovak Chemical Communication
ISSN
0010-0765
e-ISSN
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Volume of the periodical
69
Issue of the periodical within the volume
4
Country of publishing house
CZ - CZECH REPUBLIC
Number of pages
13
Pages from-to
905-917
UT code for WoS article
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EID of the result in the Scopus database
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