Enantiomeric discrimination in the NMR spectra of underivatized amino acids and α-methyl amino acids using (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid
- 1 May 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (20) , 3769-3772
- https://doi.org/10.1016/s0040-4039(00)00499-8
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- (+)-(18-Crown-6)-2,3,11,12-Tetracarboxylic Acid and Its Ytterbium(III) Complex as Chiral NMR Discriminating AgentsThe Journal of Organic Chemistry, 2000
- Nuclear magnetic resonance studies for the chiral recognition of the novel chiral stationary phase derived from 18-crown-6 tetracarboxylic acidJournal of Chromatography A, 1998
- Lanthanide-Crown Ether Mixtures as Chiral NMR Shift Reagents for Amino Acid Esters, Amines and Amino AlcoholsMagnetic Resonance in Chemistry, 1997
- Chiral recognition by 1H‐NMR, EPR, and ENDOR spectroscopyChirality, 1993
- Chiral Crown EthersTopics in Stereochemistry, 1987
- Host-guest complexation. 23. High chiral recognition of amino acid and ester guests by hosts containing one chiral elementThe Journal of Organic Chemistry, 1981