Synthesis of inherently chiral calixarenes via direct mercuration of the partial cone conformation

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22810%2F16%3A43902655" target="_blank" >RIV/60461373:22810/16:43902655 - isvavai.cz</a>

Alternative codes found

RIV/68378271:_____/16:00460528 RIV/60461373:22310/16:43902655

Result on the web

<a href="http://dx.doi.org/10.1039/c5cc09388k" target="_blank" >http://dx.doi.org/10.1039/c5cc09388k</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c5cc09388k" target="_blank" >10.1039/c5cc09388k</a>

Result language

angličtina

Original language name

Synthesis of inherently chiral calixarenes via direct mercuration of the partial cone conformation

Original language description

Direct mercuration of calix[4] arene immobilized in the partial cone conformation led to the meta-substituted isomer which was subsequently subjected to Pd-catalysed coupling (C-H activation) with the neighbouring aromatic subunit. Regioselective mercuration thus enabled access to a novel type of inherently chiral calixarenes with a highly distorted cavity potentially applicable to the design of new chiral receptors.

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

Result was created during the realization of more than one project. More information in the Projects tab.

Continuities

S - Specificky vyzkum na vysokych skolach

Publication year

2016

Confidentiality

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

Name of the periodical

Chemical Communications

ISSN

1359-7345

e-ISSN

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Volume of the periodical

52

Issue of the periodical within the volume

11

Country of publishing house

GB - UNITED KINGDOM

Number of pages

4

Pages from-to

2366-2369

UT code for WoS article

000369587800036

EID of the result in the Scopus database

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