Modular synthesis of 5-substituted thiophen-2-yl C-2'-deoxyribonucleosides
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F08%3A00309166" target="_blank" >RIV/61388963:_____/08:00309166 - 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
Modular synthesis of 5-substituted thiophen-2-yl C-2'-deoxyribonucleosides
Original language description
Title 5-substituted thiophen-2-yl C-2'-deoxyribonucleosides were prepared by cross-coupling reactions of bromothiophene C-nucleoside intermediates readily accessible by the Lewis acid mediated C-glycosidation of 2-bromothiophene.
Czech name
Modulární syntéza 5-substituovaných thiofen-2-yl C-2'-deoxyribonukleosidů
Czech description
Cílové 5-substituované thiofen-2-yl C-2'-deoxyribonukleosidy byly připraveny cross-coupling reakcemi bromthiofenových C-nukleosidových intermediátů snadno dostupných C-glycosidacemi 2-bromthiofenu působením Lewisových kyselin.
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
<a href="/en/project/LC512" target="_blank" >LC512: Center for biomolecules and complex molecular systems</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2008
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Organic Chemistry
ISSN
0022-3263
e-ISSN
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Volume of the periodical
73
Issue of the periodical within the volume
10
Country of publishing house
US - UNITED STATES
Number of pages
9
Pages from-to
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UT code for WoS article
000255698500018
EID of the result in the Scopus database
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