Additions and Corrections-The Determination of the Styryl Geometry of the 6-Styryl-4-Methoxy-2-Pyrones by Proton Magnetic Resonance SPectroscopy

1963 ◽  
Vol 28 (12) ◽  
pp. 3594-3594
Author(s):  
Peter Beak ◽  
Herbert Abelson
1989 ◽  
Vol 72 (4) ◽  
pp. 552-555
Author(s):  
George M Hanna ◽  
Cesar A Lau-Cam

Abstract Optimum experimental conditions were developed for determination of the optical purity of samples of tranylcypromine sulfate by proton magnetic resonance spectroscopy after complexation with the chiral lanthanide chelate Eu(hfc).3. At a substrate concentration of 0.25M (0.125M as sulfate) in CDC13 and an Eu(hfc)3 to substrate molar ratio of 1, the methine proton geminal to the amino group in the cyclopropane ring showed the largest induced shift and largest enantiomeric induced shift difference. From the relative intensities of the resolved (+)-CH-NH2 protons (15.77 ppm) and (-)-CH-NH2 proton (16.04 ppm), the enantiomeric purity and percentage compositions were readily calculated. The mean ± SD recovery of (+)- tranylcypromine sulfate from synthetic enantiomeric mixtures was 101.02 ± 2.59 (n = 6).


Sign in / Sign up

Export Citation Format

Share Document