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

Thomas Hjelmgaard; Olivier Roy; Lionel Nauton; Malika El-Ghozzi; Daniel Avignant; Claude Didierjean; Claude Taillefumier; Sophie Faure

doi:10.1039/c4cc00821a

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

Thomas Hjelmgaard, Olivier Roy, Lionel Nauton, Malika El-Ghozzi, Daniel Avignant, Claude Didierjean, Claude Taillefumier, Sophie Faure

Department of Chemistry

26 Citations (Scopus)

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.

Original language	English
Journal	Chemical Communications
Volume	50
Issue number	27
Pages (from-to)	3564-3567
Number of pages	4
ISSN	1359-7345
DOIs	https://doi.org/10.1039/c4cc00821a
Publication status	Published - 6 Mar 2014

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title = "Macrocyclic arylopeptoids - a novel type of cyclic N-alkylated aromatic oligoamides forming nanotubular assemblies",

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.",

author = "Thomas Hjelmgaard and Olivier Roy and Lionel Nauton and Malika El-Ghozzi and Daniel Avignant and Claude Didierjean and Claude Taillefumier and Sophie Faure",

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T1 - Macrocyclic arylopeptoids - a novel type of cyclic N-alkylated aromatic oligoamides forming nanotubular assemblies

AU - Hjelmgaard, Thomas

AU - Roy, Olivier

AU - Nauton, Lionel

AU - El-Ghozzi, Malika

AU - Avignant, Daniel

AU - Didierjean, Claude

AU - Taillefumier, Claude

AU - Faure, Sophie

PY - 2014/3/6

Y1 - 2014/3/6

N2 - 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.

AB - 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.

U2 - 10.1039/c4cc00821a

DO - 10.1039/c4cc00821a

M3 - Journal article

C2 - 24566830

SN - 1359-7345

VL - 50

SP - 3564

EP - 3567

JO - Chemical Communications

JF - Chemical Communications

IS - 27

ER -

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

Abstract

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