Issue 23, 2017

Triamide macrocyclic chloride receptors via a one-pot tandem reduction–condensation–cyclization reaction

Abstract

A pyridine containing triamide macrocycle and its substituted analog have been synthesized in one pot from the corresponding monomer without the use of coupling reagents. The macrocycle can selectively bind chloride ions. The ease of synthesis and chloride-binding properties of the macrocycle make it a highly attractive scaffold for ion-encapsulation, ion-transport and water purification.

Graphical abstract: Triamide macrocyclic chloride receptors via a one-pot tandem reduction–condensation–cyclization reaction

Associated articles

Supplementary files

Article information

Article type
Communication
Submitted
16 Mar 2017
Accepted
02 May 2017
First published
02 May 2017

Org. Biomol. Chem., 2017,15, 4937-4940

Triamide macrocyclic chloride receptors via a one-pot tandem reduction–condensation–cyclization reaction

H. Behera, V. Ramkumar and N. Madhavan, Org. Biomol. Chem., 2017, 15, 4937 DOI: 10.1039/C7OB00642J

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