Modular synthesis of 1-alpha- and 1-beta-(indol-2-yl)-2'-deoxyribose C-nucleosides

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F11%3A10104910" target="_blank" >RIV/00216208:11310/11:10104910 - isvavai.cz</a>
Alternative codes found
RIV/61388963:_____/11:00364260
Result on the web
<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2011/OB/c1ob05844d" target="_blank" >http://pubs.rsc.org/en/Content/ArticleLanding/2011/OB/c1ob05844d</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c1ob05844d" target="_blank" >10.1039/c1ob05844d</a>

Result language
angličtina
Original language name
Modular synthesis of 1-alpha- and 1-beta-(indol-2-yl)-2'-deoxyribose C-nucleosides
Original language description
A simple two-step method for the selective preparation of anomerically pure 1 alpha- and 1 beta-(indol-2-yl)deoxyribose derivatives was developed. The synthesis was based on the Sonogashira reaction of 1 alpha- and 1 beta-ethynyldeoxyribose and 2-haloanilines followed by a Pd-complex catalyzed cyclization to the corresponding indolyldeoxyribosides.
Czech name
—
Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

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)

Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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