Meta-arylation of calixarenes using organomercurial chemistry

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F13%3A00397520" target="_blank" >RIV/68378271:_____/13:00397520 - isvavai.cz</a>

Alternative codes found

RIV/60461373:22310/13:43896705 RIV/60461373:22810/13:43896705

Result on the web

<a href="http://dx.doi.org/10.1039/c3ob41085d" target="_blank" >http://dx.doi.org/10.1039/c3ob41085d</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c3ob41085d" target="_blank" >10.1039/c3ob41085d</a>

Result language

angličtina

Original language name

Meta-arylation of calixarenes using organomercurial chemistry

Original language description

A direct mercuration reaction combined with a subsequent Pd-catalyzed arylation was used to introduce the aryl moiety into the meta position of the calix[4]arene skeleton. The application of organomercurial intermediates thus allows the straightforward formation of meta-aryl-substituted derivatives representing a unique substitution pattern in calixarene chemistry.

Czech name

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Czech description

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Type

J_x - 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

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2013

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Organic & Biomolecular Chemistry

ISSN

1477-0520

e-ISSN

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Volume of the periodical

11

Issue of the periodical within the volume

33

Country of publishing house

GB - UNITED KINGDOM

Number of pages

7

Pages from-to

5528-5534

UT code for WoS article

000323141800017

EID of the result in the Scopus database

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