Efficient high-performance liquid chromatographic enantioseparation of five-membered aryl-substituted lactones and cyclic carbamates on a (R,R)-diaminodihydroethanoanthracene-derived chiral stationary phase-Reference-Cited by-同舟云学术

Efficient high-performance liquid chromatographic enantioseparation of five-membered aryl-substituted lactones and cyclic carbamates on a (R,R)-diaminodihydroethanoanthracene-derived chiral stationary phase

Published:1996-07 Issue:1 Volume:740 Page:11-19
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Maier Norbert M.,Uray Georg

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference18 articles.

1. New HPLC-chiral stationary phases for enantiomeric resolution of sulfoxides and selenoxides

2. Chromatographic optical resolution ontrans-1,2-diaminocyclohexane derivatives: Theory and applications

3. Diphenylethanediamine derivatives as chiral selectors

4. Chiral ?-substituted ?-aryloxy acetic acids: Synthesis, absolute configuration, chemical resolution, and direct separation by hplc

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

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1. Direct separation of the enantiomers of (±)-metoprolol tartrate on impregnated TLC plates withD-(−)-tartaric acid as a chiral selector;Journal of Planar Chromatography – Modern TLC;2005-08

2. A Convenient and Scaleable Synthesis of 11,12-Diamino-9,10-dihydro-9,10-ethanoanthracene and Its Enantiomers;Synthesis;2005

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4. Evaluation of two pairs of chiral stationary phases: Effects from the length of the achiral spacers;Chirality;2004

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