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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

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • 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