Chiral recognition ability and solvent versatility of bonded amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase: Enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs

Ashraf Ghanem; Ebtessam Al-Humaidi

doi:10.1002/chir.20398

Chiral recognition ability and solvent versatility of bonded amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase: Enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs

Chirality ◽

10.1002/chir.20398 ◽

2007 ◽

Vol 19 (6) ◽

pp. 477-484 ◽

Cited By ~ 4

Author(s):

Ashraf Ghanem ◽

Ebtessam Al-Humaidi

Keyword(s):

Stationary Phase ◽

Chiral Recognition ◽

Chiral Stationary Phase ◽

Recognition Ability ◽

Chromatographic Resolution ◽

Liquid Chromatographic

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Chiral recognition models for the liquid chromatographic resolution of π-acidic racemates on a chiral stationary phase derived from N-phenyl-N-alkylamide of (S-naproxen)

Journal of Chromatography A ◽

10.1016/s0021-9673(96)00508-0 ◽

1996 ◽

Vol 752 (1-2) ◽

pp. 77-84 ◽

Cited By ~ 15

Author(s):

Myung Ho Hyun ◽

Myeong Seon Na ◽

Jong Sung Jin

Keyword(s):

Stationary Phase ◽

Chiral Recognition ◽

Chiral Stationary Phase ◽

Chromatographic Resolution ◽

Liquid Chromatographic

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Effect of the residual silanol group protection on the liquid chromatographic resolution of α-amino acids and proton pump inhibitors on a ligand exchange chiral stationary phase

Journal of Separation Science ◽

10.1002/jssc.201300079 ◽

2013 ◽

Vol 36 (8) ◽

pp. 1349-1355 ◽

Cited By ~ 8

Author(s):

Dong Hee Ma ◽

Jong Sung Jin ◽

Euh Duck Jeong ◽

Myung Ho Hyun

Keyword(s):

Amino Acids ◽

Stationary Phase ◽

Proton Pump Inhibitors ◽

Proton Pump ◽

Ligand Exchange ◽

Chiral Stationary Phase ◽

Silanol Group ◽

Chromatographic Resolution ◽

Liquid Chromatographic ◽

Residual Silanol Group

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Chiral Recognition Ability of an Optically Active Poly(diphenylacetylene) as a Chiral Stationary Phase for HPLC

Chemistry Letters ◽

10.1246/cl.160542 ◽

2016 ◽

Vol 45 (9) ◽

pp. 1063-1065 ◽

Cited By ~ 23

Author(s):

Katsuhiro Maeda ◽

Miyuki Maruta ◽

Kouhei Shimomura ◽

Tomoyuki Ikai ◽

Shigeyoshi Kanoh

Keyword(s):

Stationary Phase ◽

Chiral Recognition ◽

Chiral Stationary Phase ◽

Optically Active ◽

Recognition Ability

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Examples of liquid chromatographic resolution of π-acidic racemates on a π-acidic chiral stationary phase

Journal of High Resolution Chromatography ◽

10.1002/jhrc.1240180114 ◽

1995 ◽

Vol 18 (1) ◽

pp. 63-65 ◽

Cited By ~ 3

Author(s):

Myung Ho Hyun ◽

Chung Sik Min ◽

Yoon Jae Cho

Keyword(s):

Stationary Phase ◽

Chiral Stationary Phase ◽

Chromatographic Resolution ◽

Liquid Chromatographic

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Liquid Chromatographic Resolution of N-(3,5-Dinitrobenzoyl)-α-amino Acids on a New Chiral Stationary Phase: the First Liquid Chromatographic Utilization of a Double-Ureide Pocket for the Recognition of Chiral Carboxylate Anions

Bulletin of the Korean Chemical Society ◽

10.5012/bkcs.2007.28.11.1980 ◽

2007 ◽

Vol 28 (11) ◽

pp. 1980-1984 ◽

Cited By ~ 1

Keyword(s):

Amino Acids ◽

Stationary Phase ◽

Chiral Stationary Phase ◽

Carboxylate Anions ◽

Chromatographic Resolution ◽

Liquid Chromatographic

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ChemInform Abstract: Liquid Chromatographic Resolution of Racemic Ketones as Their Oxime 3,5-Dinitrophenyl Carbamates on a Chiral Stationary Phase.

ChemInform ◽

10.1002/chin.198912332 ◽

1989 ◽

Vol 20 (12) ◽

Author(s):

M. H. HYUN ◽

Y.-W. PARK ◽

I.-K. BAIK

Keyword(s):

Stationary Phase ◽

Chiral Stationary Phase ◽

Chromatographic Resolution ◽

Liquid Chromatographic

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ChemInform Abstract: A Chiral Stationary Phase Derived from (R,R)-Tartramide with Broadened Scope of Application to the Liquid Chromatographic Resolution of Enantiomers.

ChemInform ◽

10.1002/chin.198749360 ◽

1987 ◽

Vol 18 (49) ◽

Author(s):

Y. DOBASHI ◽

S. HARA

Keyword(s):

Stationary Phase ◽

Chiral Stationary Phase ◽

Resolution Of Enantiomers ◽

Scope Of Application ◽

Chromatographic Resolution ◽

Liquid Chromatographic

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New ligand exchange chiral stationary phase for the liquid chromatographic resolution of α- and β-amino acids

Journal of Chromatography A ◽

10.1016/s0021-9673(03)00276-0 ◽

2003 ◽

Vol 992 (1-2) ◽

pp. 47-56 ◽

Cited By ~ 41

Author(s):

Myung Ho Hyun ◽

Sang Cheol Han ◽

Sung Hee Whangbo

Keyword(s):

Amino Acids ◽

Stationary Phase ◽

Ligand Exchange ◽

Chiral Stationary Phase ◽

Chromatographic Resolution ◽

Liquid Chromatographic

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ChemInform Abstract: A New Chiral Stationary Phase Derived from Cyclohexylamide Derivative of (S)-Naproxen for the Liquid Chromatographic Resolution of Enantiomers

ChemInform ◽

10.1002/chin.199619037 ◽

2010 ◽

Vol 27 (19) ◽

pp. no-no

Author(s):

M. H. HYUN ◽

J. B. LEE

Keyword(s):

Stationary Phase ◽

Chiral Stationary Phase ◽

Resolution Of Enantiomers ◽

Chromatographic Resolution ◽

Liquid Chromatographic

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High-performance liquid chromatographic resolution of racemic 1,4-benzodiazepin-2-ones by means of a β-cyclodextrin silica bonded chiral stationary phase

Journal of Chromatography A ◽

10.1016/s0021-9673(01)91610-3 ◽

1990 ◽

Vol 506 ◽

pp. 617-625 ◽

Cited By ~ 20

Author(s):

C. Bertucci ◽

E. Domenici ◽

G. Uccello-Barretta ◽

P. Salvadori

Keyword(s):

Stationary Phase ◽

High Performance ◽

Chiral Stationary Phase ◽

High Performance Liquid Chromatographic ◽

Chromatographic Resolution ◽

Liquid Chromatographic

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