Issue 98, 2012

Design and synthesis of regioisomeric triazole based peptidomimeticmacrocycles and their dipole moment controlled self-assembly

Abstract

Two peptidomimetic macrocycles, regioisomeric in terms of the position of triazole/amide, have been synthesized. Both undergo self-assembly in a parallel manner but in solvents of opposite polarity, ascribed to (β, β) and (β-D, β-L) hydrogen bonding leading to formation of two different unique classes of organic nanostructures.

Graphical abstract: Design and synthesis of regioisomeric triazole based peptidomimetic macrocycles and their dipole moment controlled self-assembly

Supplementary files

Article information

Article type
Communication
Submitted
10 Sep 2012
Accepted
25 Oct 2012
First published
26 Oct 2012

Chem. Commun., 2012,48, 11975-11977

Design and synthesis of regioisomeric triazole based peptidomimetic macrocycles and their dipole moment controlled self-assembly

A. Ghorai, E. Padmanaban, C. Mukhopadhyay, B. Achari and P. Chattopadhyay, Chem. Commun., 2012, 48, 11975 DOI: 10.1039/C2CC36566A

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