meta-Bridged calix[4] arenes: a straightforward synthesis via organomercurial chemistry

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F13%3A43896704" target="_blank" >RIV/60461373:22310/13:43896704 - isvavai.cz</a>
Alternative codes found
RIV/60461373:22810/13:43896704
Result on the web
<a href="http://dx.doi.org/10.1039/c3cc43284j" target="_blank" >http://dx.doi.org/10.1039/c3cc43284j</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c3cc43284j" target="_blank" >10.1039/c3cc43284j</a>

Result language
angličtina
Original language name
meta-Bridged calix[4] arenes: a straightforward synthesis via organomercurial chemistry
Original language description
The regioselective mercuration of tetraalkylated calix[4]arenes with Hg(OCOCF3)(2) leads to the formation of meta-substituted products which enabled Pd-catalysed intramolecular bridging within the calixarene skeleton. Bridged derivatives represent a completely novel substitution pattern in calixarene chemistry with extremely distorted cavities and possible applications in supramolecular chemistry.
Czech name
—
Czech description
—

Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

Project
<a href="/en/project/GAP207%2F12%2F2027" target="_blank" >GAP207/12/2027: Synthesis and applications of inherently chiral calixarenes</a><br>
Continuities
S - Specificky vyzkum na vysokych skolach

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

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