Issue 9, 2016

Synthesis and characterization of chiral aza-macrocycles and study of their enantiomer recognition ability for organo-phosphoric acid and phosphonic acid derivatives by 31P NMR and fluorescence spectroscopy

Abstract

Two diastereomers of optically active N,O-containing new macrocycles with dual chirality of the ring and pendent group were synthesized and characterized. The difference in the accessibility of the cavity was explored to discriminate the enantiomers of the derivatives of organo-phosphoric and phosphonic acids by 31P NMR and fluorescence spectroscopy.

Graphical abstract: Synthesis and characterization of chiral aza-macrocycles and study of their enantiomer recognition ability for organo-phosphoric acid and phosphonic acid derivatives by 31P NMR and fluorescence spectroscopy

Supplementary files

Article information

Article type
Paper
Submitted
20 Dec 2015
Accepted
28 Jan 2016
First published
28 Jan 2016

Org. Biomol. Chem., 2016,14, 2742-2748

Synthesis and characterization of chiral aza-macrocycles and study of their enantiomer recognition ability for organo-phosphoric acid and phosphonic acid derivatives by 31P NMR and fluorescence spectroscopy

A. N. Khanvilkar and A. V. Bedekar, Org. Biomol. Chem., 2016, 14, 2742 DOI: 10.1039/C5OB02616D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements