Synthesis of racemic 2-hydroxy-4- and 2-hydroxy-5-(hydroxymethyl)cyclohexane pyrimidine C-nucleoside analogues

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F04%3A00100876" target="_blank" >RIV/61388963:_____/04:00100876 - 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 racemic 2-hydroxy-4- and 2-hydroxy-5-(hydroxymethyl)cyclohexane pyrimidine C-nucleoside analogues
Original language description
New racemic 2-hydroxy-4- and 2-hydroxy-5-(hydroxymethyl)cyclohexane analogues of pseudouridine, 2-thiopseudouridine, pseudoisocytidine, and pseudocytidine were prepared from 3-(benzyloxy)methyl-7-oxabicyclo[4.1.0]heptane
Czech name
Synthesa racemických analog 2-hydroxy-4- a 2-hydroxy-5-(hydroxymethyl)cyklohexan pyrimidinových C-nukleosidů
Czech description
Nová racemická 2-hydroxy-4- and 2-hydroxy-5-(hydroxymethyl)cyklohexanová analoga pseudouridinu, 2-thiopseudouridinu, pseudoisocytidinu a pseudocytidinu byla připravena z 3-(benzyloxy)methyl-7-oxabicyklo[4.1.0]heptanu

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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