Direct meta substitution of calix[4]arenes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F22%3A43924479" target="_blank" >RIV/60461373:22310/22:43924479 - isvavai.cz</a>
Result on the web
<a href="https://pubs.rsc.org/en/content/articlelanding/2022/OB/D2OB01437H" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2022/OB/D2OB01437H</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/d2ob01437h" target="_blank" >10.1039/d2ob01437h</a>
Alternative languages
Result language
angličtina
Original language name
Direct meta substitution of calix[4]arenes
Original language description
Calixarenes represent very popular building blocks in supramolecular chemistry. Compared to other macrocyclic families, they exhibit an almost infinite possibility of derivatization of the basic skeleton, which makes them ideal candidates for the design of new receptors or other functional systems. Although the chemistry of calixarenes is well established, there are still some substitution patterns that are unavailable or require a very lengthy synthetic approach. Among such synthetic challenges is the meta substitution of the aromatic skeleton (relative to phenolic oxygen), which, in conjunction with the 3D structure of calixarenes, leads to the inherent chirality and enables the synthesis of derivatives with a hitherto undescribed topology. This review deals with the current achievements in the meta substitution of calixarenes.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10401 - Organic chemistry
Result continuities
Project
<a href="/en/project/GA20-08667S" target="_blank" >GA20-08667S: Chemistry of phenoxathiin-based thicalixarenes and related compounds</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Organic and Biomolecular Chemistry
ISSN
1477-0520
e-ISSN
1477-0539
Volume of the periodical
20
Issue of the periodical within the volume
37
Country of publishing house
GB - UNITED KINGDOM
Number of pages
14
Pages from-to
7377-7390
UT code for WoS article
000851576000001
EID of the result in the Scopus database
2-s2.0-85139375122