Introducing an amine group to calix[5]arene: comparison of several methods

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F16%3A43901553" target="_blank" >RIV/60461373:22310/16:43901553 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1080/10610278.2015.1119275" target="_blank" >http://dx.doi.org/10.1080/10610278.2015.1119275</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1080/10610278.2015.1119275" target="_blank" >10.1080/10610278.2015.1119275</a>

Result language
angličtina
Original language name
Introducing an amine group to calix[5]arene: comparison of several methods
Original language description
Chemists often use an amine group as an intermediate in syntheses of imines, amides and ureas; however, in the case of syntheses of p-aminophenol type compounds, several problems might occur. In this article, we prepared p-aminocalix[5]arene-pentaol by reduction of both nitro and azo derivatives, and compared four methods of the amine preparation, focusing mainly on its gramme scale and time-consuming issues.
Czech name
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Czech description
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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/GP14-24880P" target="_blank" >GP14-24880P: Synthesis of Ligands for Interactions with Tetrameric and Pentameric Proteins</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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