Issue 44, 2015

Conformational promiscuity in triazolamers derived from quaternary amino acids mimics peptide behaviour

Abstract

1,4-Substituted triazole oligomers made from quaternary amino acid derivatives present a conformational behaviour with similarities to that of natural peptides. Twisted strand and zig-zag type conformations have both been obtained in the crystal state. In a solution signs of weakly ordered structures have been detected depending on the substituents and the solvents used.

Graphical abstract: Conformational promiscuity in triazolamers derived from quaternary amino acids mimics peptide behaviour

Supplementary files

Article information

Article type
Communication
Submitted
16 Jul 2015
Accepted
02 Oct 2015
First published
02 Oct 2015

Org. Biomol. Chem., 2015,13, 10797-10801

Author version available

Conformational promiscuity in triazolamers derived from quaternary amino acids mimics peptide behaviour

J. Solà, M. Bolte and I. Alfonso, Org. Biomol. Chem., 2015, 13, 10797 DOI: 10.1039/C5OB01461A

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