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Journal ArticleDOI

Considerations of Chiral Recognition Relevant to the Liquid Chromatographic Separation of Enantiomers

William H. Pirkle, +1 more
- 01 Aug 1989 - 
- Vol. 20, Iss: 31
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This article is published in ChemInform.The article was published on 1989-08-01. It has received 67 citations till now.

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Marfey’s reagent for chiral amino acid analysis: A review

TL;DR: Characteristics and application of Marfey’s reagent (MR) including general protocols for synthesis of the reagent and diastereomers along with advantages, disadvantages and the required precautions are described.
Journal ArticleDOI

Preparative chiral chromatographic resolution of enantiomers in drug discovery.

TL;DR: The most suitable types of chiral stationary phases (CSPs) available for this purpose are discussed with special reference to loadability and compatibility with different mobile phase systems.
Journal ArticleDOI

Effect of reaction pH on enolization and racemization reactions of glucose and fructose on heating with amino acid enantiomers and formation of melanoidins as result of the Maillard reaction.

TL;DR: This study investigates the effect of reaction pH on enolization and racemization reactions of glucose and fructose on heating with amino acid enantiomers, can influence the formation of melanoidins as result of the Maillard reaction.
Journal ArticleDOI

Chiral pharmaceuticals in the environment

TL;DR: Despite the great importance of the stereochemistry in pharmaceutical science, pharmacology and organic chemistry, this is normally neglected in environmental studies, therefore, CP in the environment need much more attention from the scientific community, and more research is required.
Journal ArticleDOI

Optical Resolution of Racemic Mixtures of Amino Acids through Nanofiltration Membrane Process

TL;DR: In this paper, an optical resolution of racemic mixtures of arginine and alanine was performed by chiral selective nanofiltration membrane, which was prepared by interfacial polymerization of metaphenylenediamine, trimesoyl chloride, and S (-)-2-acetoxypropionyl chloride.
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