Determination of Enantiomeric Purity for Chiral π‐Basic Aromatic Alcohols Chiral Samples by 1 H NMR Spectroscopy

2019 ◽  
Vol 41 (1) ◽  
pp. 4-9 ◽  
Author(s):  
Kyu Sung Heo ◽  
Jae Jeong Ryoo
1992 ◽  
Vol 47 (7) ◽  
pp. 1034-1036 ◽  
Author(s):  
Bernhard Koppenhoefer ◽  
Michael Hummel

Enantiomers of N-trifluoroacetyl-amino acid methyl esters in CC14 solution, after addition of the chiral polysiloxane (L)-Chirasil-Val, display a chemical shift nonequivalence ΔΔδ in both 1H NMR and 19F NMR spectroscopy. The effects found for the leucine and valine derivatives can be correlated with the thermodynamic parameters of interaction in the undiluted system, as determined by gas chromatography. In CDC13 solution, no peak splitting was observed. The method is potentially useful for the determination of the enantiomeric purity of substrates of low volatility.


Chirality ◽  
2013 ◽  
Vol 25 (11) ◽  
pp. 780-786 ◽  
Author(s):  
Jordi Redondo ◽  
Anna Capdevila ◽  
Sonia Ciudad

1988 ◽  
Vol 53 (24) ◽  
pp. 5768-5770 ◽  
Author(s):  
Piero Salvadori ◽  
Gloria Uccello-Barretta ◽  
Sergio Bertozzi ◽  
Roberta Settambolo ◽  
Raffaello Lazzaroni

2008 ◽  
Vol 46 (11) ◽  
pp. 1051-1054 ◽  
Author(s):  
Vinicius M. Mello ◽  
Flavia C. C. Oliveira ◽  
William G. Fraga ◽  
Claudia J. do Nascimento ◽  
Paulo A. Z. Suarez

ChemInform ◽  
1989 ◽  
Vol 20 (20) ◽  
Author(s):  
P. SALVADORI ◽  
G. UCCELLO-BARRETTA ◽  
S. BERTOZZI ◽  
R. SETTAMBOLO ◽  
R. LAZZARONI

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