(+)-BINOL and pure shift experiment: A bidirectional approach for NMR chiral discrimination of overcrowded spectra of primary amines

10Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

In this work, enantiopure 1,1'-bi-2-naphthol (BINOL) derivatives and carboxylic acids were evaluated as chiral solvating agents (CSAs) in the nuclear magnetic resonance (NMR) chiral discrimination of primary amines. Among the CSAs screened, the readily available (+)-BINOL revealed a simple and rapid chiral auxiliary for 1H NMR chiral discrimination. The procedure required few minutes, assigning of the absolute configuration. The protocol was improved using the 1H pure shift pulse sequence for overcrowded alkyl primary amines due to the absence of JHH couplings. The 1H pure shift NMR experiment and the readily available (+)-BINOL chiral auxiliary can be used for routine chiral discrimination analysis of complex NMR spectra. Printed in Brazil-

Cite

CITATION STYLE

APA

Merino, J. C., Keppler, A. F., & Silva, M. S. (2018). (+)-BINOL and pure shift experiment: A bidirectional approach for NMR chiral discrimination of overcrowded spectra of primary amines. Journal of the Brazilian Chemical Society, 29(8), 1638–1644. https://doi.org/10.21577/0103-5053.20180035

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free