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Behera H, Ramkumar V, Madhavan N. Triamide macrocyclic chloride receptors via a one-pot tandem reduction-condensation-cyclization reaction. Org Biomol Chem. 2017;15(23):4937-4940doi: 10.1039/c7ob00642j.
Behera, H., Ramkumar, V., & Madhavan, N. (2017). Triamide macrocyclic chloride receptors via a one-pot tandem reduction-condensation-cyclization reaction. Organic & biomolecular chemistry, 15(23), 4937-4940. https://doi.org/10.1039/c7ob00642j
Behera, Harekrushna, et al. "Triamide macrocyclic chloride receptors via a one-pot tandem reduction-condensation-cyclization reaction." Organic & biomolecular chemistry vol. 15,23 (2017): 4937-4940. doi: https://doi.org/10.1039/c7ob00642j
Behera H, Ramkumar V, Madhavan N. Triamide macrocyclic chloride receptors via a one-pot tandem reduction-condensation-cyclization reaction. Org Biomol Chem. 2017 Jun 14;15(23):4937-4940. doi: 10.1039/c7ob00642j. PMID: 28485420.
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Org Biomol Chem. 2017 Jun 14;15(23):4937-4940. doi: 10.1039/c7ob00642j.

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

Organic & biomolecular chemistry

Harekrushna Behera, Venkatachalam Ramkumar, Nandita Madhavan

Affiliations

  1. Department of Chemistry, Indian Institute of Technology, Madras, Chennai, Tamil Nadu 600036, India. [email protected].

PMID: 28485420 DOI: 10.1039/c7ob00642j

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.

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