H-1 AND C-13 NMR DETERMINATION OF THE ENANTIOMERIC PURITY OF SUBSTITUTED 4-AMINO-3-(THIEN-2-YL)-BUTYRIC ACIDS AND 4-AMINO-3-(BENZO[B]FURAN-2-YL)-BUTYRIC ACIDS, LIGANDS OF THE GABA(B) RECEPTOR
S. Alakoumebrik et al., H-1 AND C-13 NMR DETERMINATION OF THE ENANTIOMERIC PURITY OF SUBSTITUTED 4-AMINO-3-(THIEN-2-YL)-BUTYRIC ACIDS AND 4-AMINO-3-(BENZO[B]FURAN-2-YL)-BUTYRIC ACIDS, LIGANDS OF THE GABA(B) RECEPTOR, Spectroscopy letters, 31(5), 1998, pp. 925-944
The enantiomeric composition and absolute configuration of 4-Amino-3-(
benzo[b]furan-2-yl)- Butanoic Acids and of 4-Amino-3-(thien-2-yl)- But
anoic Acids 1 may be accurately determined by H-1 and C-13 nuclear mag
netic resonance analysis of the corresponding derivatives 3 prepared b
y reaction with chiral reagents. Correlation with HPLC is signaled.