Norbornane as the novel pseudoglycone moiety in nucleosides
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F09%3A00331982" target="_blank" >RIV/61388963:_____/09:00331982 - 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
Norbornane as the novel pseudoglycone moiety in nucleosides
Original language description
This study concerns synthesis of novel racemic conformationally locked nucleosides with bicyclo[2.2.1]heptene or heptane ring system substituted with nucleobase at position 7 and with the anti-configuration of the nucleobase. Biological activity of the newly prepared compounds is described. Activity against Coxsackie B3 virus is discussed.
Czech name
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Czech description
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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
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2009
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Tetrahedron
ISSN
0040-4020
e-ISSN
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Volume of the periodical
65
Issue of the periodical within the volume
45
Country of publishing house
GB - UNITED KINGDOM
Number of pages
9
Pages from-to
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UT code for WoS article
000271094000030
EID of the result in the Scopus database
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