Synthesis of novel racemic carbocyclic nucleosides derived from 5,6-disubstituted norbornene
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F10%3A00342649" target="_blank" >RIV/61388963:_____/10:00342649 - 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 novel racemic carbocyclic nucleosides derived from 5,6-disubstituted norbornene
Original language description
This study concerns synthesis of novel racemic conformationally locked nucleosides with bicyclo[2.2.1]heptene ring system substituted with nucleobase and hydroxymethyl group at positions 5 and 6 and their derivatives (saturated a cis-hydroxylated compounds). Biological activity of the newly prepared compounds is described.
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
2010
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 Communications
ISSN
0010-0765
e-ISSN
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Volume of the periodical
75
Issue of the periodical within the volume
1
Country of publishing house
CZ - CZECH REPUBLIC
Number of pages
20
Pages from-to
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UT code for WoS article
000274668100001
EID of the result in the Scopus database
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