Issue 11, 2015

Chiral discrimination of β-telluride carboxylic acids by NMR spectroscopy

Abstract

In this work, the nuclei (1H and 125Te) for NMR spectroscopy and enantiopure compounds as chiral solvent agents (CSAs) and chiral derivatisation agents (CDAs) were evaluated under different conditions. The structure of β-telluride carboxylic acids was also modified to observe the effect on anisochrony.

Graphical abstract: Chiral discrimination of β-telluride carboxylic acids by NMR spectroscopy

Supplementary files

Article information

Article type
Letter
Submitted
17 Jul 2015
Accepted
27 Aug 2015
First published
01 Sep 2015

New J. Chem., 2015,39, 8240-8244

Author version available

Chiral discrimination of β-telluride carboxylic acids by NMR spectroscopy

M. S. Silva and D. Pietrobom, New J. Chem., 2015, 39, 8240 DOI: 10.1039/C5NJ01877C

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