Title
LFER and CoMFA studies on optical resolution of α-alkyl α-aryloxy acetic acid methyl esters on DACH-DNB chiral stationary phase
Abstract
The HPLC resolution of a series of racemic a-substituted a-aryloxy acetic acid methyl esters I on a p-acid chiral stationary phase containing N,N'-(3,5-dinitrobenzoyl)-trans-1,2-diaminocyclohexane as chiral selector was modelled by linear free energy-related (LFER) equations and comparative molecular field analysis (CoMFA). Our results indicate that the retention process mainly depends on solute lipophilicity and steric properties, whereas enantioselectivity is primarily influenced by electrostatic and steric interactions. CoMFA provided additional information with respect to the LFER study, allowed the mixing of different subsets of I and led to a quantitative 3D model of steric and electrostatic factors responsible for chiral recognition.
Year
DOI
Venue
1995
10.1007/BF00124403
Journal of Computer-Aided Molecular Design
Keywords
Field
DocType
Chiral chromatography,Enantioseparation,CoMFA,3D QSAR
Chirality (chemistry),Alkyl,Chiral column chromatography,Taft equation,Computational chemistry,Chemistry,Steric effects,Lipophilicity,Acetic acid,High-performance liquid chromatography
Journal
Volume
Issue
ISSN
9
2
0920-654X
Citations 
PageRank 
References 
0
0.34
1
Authors
8