Second generation of calix[6]aza-Cryptands: synthesis of heteroditopic receptors for organic ion pairs.
Identifieur interne : 000248 ( PubMed/Corpus ); précédent : 000247; suivant : 000249Second generation of calix[6]aza-Cryptands: synthesis of heteroditopic receptors for organic ion pairs.
Auteurs : Stéphane Le Gac ; Mickaël Ménand ; Ivan JabinSource :
- Organic letters [ 1523-7052 ] ; 2008.
English descriptors
- KwdEn :
- MESH :
- chemical , chemical synthesis : Calixarenes, Ethers, Cyclic.
- chemical , chemistry : Methenamine.
- Magnetic Resonance Spectroscopy.
Abstract
The efficient syntheses of calix[6]azacryptands decorated with anion-binding groups on the narrow rim have been achieved from an 1,3,5-tris-protected calix[6]hexa-amine. These heteroditopic receptors can bind ammonium ions or organic ion pair salts with a positive cooperativity. In regard to their functionalization at the 1,3,5-phenolic positions, these compounds constitute the first examples of a second generation of C3 v symmetrical calix[6]azacryptands.
DOI: 10.1021/ol8021726
PubMed: 18939804
Links to Exploration step
pubmed:18939804Le document en format XML
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<author><name sortKey="Menand, Mickael" sort="Menand, Mickael" uniqKey="Menand M" first="Mickaël" last="Ménand">Mickaël Ménand</name>
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<author><name sortKey="Jabin, Ivan" sort="Jabin, Ivan" uniqKey="Jabin I" first="Ivan" last="Jabin">Ivan Jabin</name>
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<series><title level="j">Organic letters</title>
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<front><div type="abstract" xml:lang="en">The efficient syntheses of calix[6]azacryptands decorated with anion-binding groups on the narrow rim have been achieved from an 1,3,5-tris-protected calix[6]hexa-amine. These heteroditopic receptors can bind ammonium ions or organic ion pair salts with a positive cooperativity. In regard to their functionalization at the 1,3,5-phenolic positions, these compounds constitute the first examples of a second generation of C3 v symmetrical calix[6]azacryptands.</div>
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<Title>Organic letters</Title>
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<Abstract><AbstractText>The efficient syntheses of calix[6]azacryptands decorated with anion-binding groups on the narrow rim have been achieved from an 1,3,5-tris-protected calix[6]hexa-amine. These heteroditopic receptors can bind ammonium ions or organic ion pair salts with a positive cooperativity. In regard to their functionalization at the 1,3,5-phenolic positions, these compounds constitute the first examples of a second generation of C3 v symmetrical calix[6]azacryptands.</AbstractText>
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