Chiral recognition in gas chromatogaphy by diamide-diamide solute-solvent interaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry
Reference13 articles.
1. Interaction between asymmetric solutes and solvents
2. Separation of enantiomers on packed columns containing optically active diamide phases
3. N-docosanoyl-l-valine-2-(2-methyl)-n-heptadecylamide as a stationary phase for the resolution of optical isomers in gas-liquid chromatography
4. Shu-Cheng Chang, R. Charles and E. Gil-Av, Poster presented at the Franco-Israeli Symposium on Chiral Structures, Milly La Forét, May 1979.
5. S.-C. Chang, R. Charles and E. Gil-Av. to be published.
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1. Gas chromatographic enantiomer separation on a chiral self-associating selector;Journal of Chromatography A;1996-10
2. Enantiomer separation of amino acids as theirN-alkyloxycarbonyl alkylamide derivatives by chiral phase capillary GC;Journal of High Resolution Chromatography;1996-09
3. N-Alkyloxycarbonyl Isobutylamides as Readily Prepared Diamide Derivatives of Amino Acids for Separation of Enantiomeric Isomers by Chiral Phase Capillary Gas Chromatography;Chemistry Letters;1995-04
4. Preparative separation of amino acid enantiomers asN-TFA,O-isopropyl derivatives by continuous countercurrent gas-liquid chromatography;Chirality;1993
5. Chiral bonded packings for liquid chromatography: Preparation and evaluation of N-acylated aminoacid packings based on aminopropylated silica gel;Chromatographia;1989-08
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