Diphenylethanediamine (DPEDA) derivatives as chiral selectors: IV. A comparison of 3,5-dinitrobenzoylated (S,S)- and (S,R)-DPEDA-derived chiral stationary phases with Pirkle's standard (R)-phenylglycine-derived phase in normal phase HPLC-Reference-Cited by-同舟云学术

Diphenylethanediamine (DPEDA) derivatives as chiral selectors: IV. A comparison of 3,5-dinitrobenzoylated (S,S)- and (S,R)-DPEDA-derived chiral stationary phases with Pirkle's standard (R)-phenylglycine-derived phase in normal phase HPLC

Published:1994 Issue:2 Volume:6 Page:116-128
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Maier Norbert M.,Uray Georg,Kleidernigg Oliver P.,Lindner Wolfgang

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference24 articles.

1. Diphenylethanediamine (DPEDA) derivatives as chiral selectors. III. A comparison of four new diastereomeric chiral stationary phases prepared by addition of mono-3,5-dinitrobenzoyl-DPEDA derivatives to optically pure epoxy silica. J. Chromatogr., in press, 1994.

2. An improved chiral stationary phase for the facile separation of enantiomers

3. Design, synthesis, and evaluation of an improved enantioselective naproxen selector

4. Chromatographic resolution of 1,2-amino alcohols on a chiral stationary phase containing N,N′-(3,5-dinitrobenzoyl)-trans-1,2-diaminocyclohexane

5. Direct enantiomeric separation of β-blockers on ChyRoSine-a by supercritical fluid chromatography: Supercritical carbon dioxide as transient in situ derivatizing agent

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