Calix[4]arenes with intramolecularly bridged meta positions prepared via Pd-catalysed double C-H activation

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F13%3A43896703" target="_blank" >RIV/60461373:22310/13:43896703 - isvavai.cz</a>
Alternative codes found
RIV/60461373:22340/13:43896703 RIV/60461373:22810/13:43896703
Result on the web
<a href="http://dx.doi.org/10.1039/c3cc40655e" target="_blank" >http://dx.doi.org/10.1039/c3cc40655e</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c3cc40655e" target="_blank" >10.1039/c3cc40655e</a>

Result language
angličtina
Original language name
Calix[4]arenes with intramolecularly bridged meta positions prepared via Pd-catalysed double C-H activation
Original language description
The introduction of a 2-pyridylsulfoxide moiety into the upper rim of calix[4]arenes enabled the synthesis of unprecedented derivatives with intramolecularly bridged meta positions of two neighbouring aromatic subunits. Palladium-catalysed double C-H activation thus represents a straightforward way to a completely novel type of calixarenes.
Czech name
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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
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Project
<a href="/en/project/GAP207%2F12%2F2027" target="_blank" >GAP207/12/2027: Synthesis and applications of inherently chiral calixarenes</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Result description