Issue 27, 2014
From the journal:

Chemical Communications

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

Thomas Hjelmgaard,‡*a   Olivier Roy,bc   Lionel Nauton,bc   Malika El-Ghozzi,bc   Daniel Avignant,bc   Claude Didierjean,de   Claude Taillefumierbc  and  Sophie Faure*bc  

* Corresponding authors

a Department of Chemistry, Section for Chemical Biology and Nanoscience, Faculty of Science, University of Copenhagen, Thorvaldsensvej 40, 1871 Frederiksberg C, Denmark

b Clermont Université, Université Blaise Pascal, Institut de Chimie de Clermont-Ferrand, BP 10448, 63000 Clermont-Ferrand, France

c CNRS, UMR 6296, ICCF, BP 80026, 63171 Aubière Cedex, France
E-mail: Sophie.Faure@univ-bpclermont.fr
Fax: +33 (0)4 73 40 77 17
Tel: +33 (0)4 73 40 52 25

d Université de Lorraine, CRM2, UMR 7036, Vandoeuvre-les-Nancy, France

e CNRS, CRM2, UMR 7036, Vandoeuvre-les-Nancy, France

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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Article information

DOI
https://doi.org/10.1039/C4CC00821A
Article type
Communication
Submitted
30 Jan 2014
Accepted
10 Feb 2014
First published
10 Feb 2014

Chem. Commun., 2014,50, 3564-3567

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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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