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Issue 27, 2014
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Macrocyclic arylopeptoids – a novel type of cyclic N-alkylated aromatic oligoamides forming nanotubular assemblies

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Abstract

The head-to-tail conversion of linear arylopeptoids (oligomeric N-substituted aminomethyl benzamides) into the derived novel macrocycles has enabled the first X-ray structures of arylopeptoid constructs and the identification of well-defined architectures in solution.

Graphical abstract: Macrocyclic arylopeptoids – a novel type of cyclic N-alkylated aromatic oligoamides forming nanotubular assemblies

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Supplementary files

Article information


Submitted
30 Jan 2014
Accepted
10 Feb 2014
First published
10 Feb 2014

Chem. Commun., 2014,50, 3564-3567
Article type
Communication
Author version available

Macrocyclic arylopeptoids – a novel type of cyclic N-alkylated aromatic oligoamides forming nanotubular assemblies

T. Hjelmgaard, O. Roy, L. Nauton, M. El-Ghozzi, D. Avignant, C. Didierjean, C. Taillefumier and S. Faure, Chem. Commun., 2014, 50, 3564
DOI: 10.1039/C4CC00821A

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