Separation of some enantiomeric di- and tripeptides on chiral stationary phases.
J Chromatogr
; 398: 203-9, 1987 Jul 10.
Article
en En
| MEDLINE
| ID: mdl-3654838
ABSTRACT
The chromatographic behavior of the N-3,5-dinitrobenzoyl derivatives of twelve dipeptide esters and two tripeptide esters was investigated on three different chiral stationary phases (CSPs). It is observed that the stereoisomers present in each sample may be cleanly separated on each chiral phase. A degree of regularity is noted in the elution order of the enantiomers and often of the diastereomers. Elution order of the enantiomers is related to a chiral recognition model for each CSP.
Buscar en Google
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Oligopéptidos
/
Dipéptidos
Idioma:
En
Revista:
J Chromatogr
Año:
1987
Tipo del documento:
Article