Enantiomeric separation of amino acids by micro high-performance liquid chromatography on an l-proline-bonded stationary phase

Journal of Chromatography A ◽

10.1016/s0021-9673(01)92612-3 ◽

1987 ◽

Vol 407 ◽

pp. 151-158 ◽

Author(s):

Toyohide Takeuchi ◽

Homare Asai ◽

Daido Ishii

Keyword(s):

Amino Acids ◽

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

Stationary Phase ◽

High Performance ◽

Enantiomeric Separation

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Enantiomeric separation of five amino acids by high-performance liquid chromatography on a chiral crown ether column

Chirality ◽

10.1002/(sici)1520-636x(1997)9:2<150::aid-chir13>3.0.co;2-m ◽

1997 ◽

Vol 9 (2) ◽

pp. 150-152 ◽

Author(s):

Fran�ois Gimenez ◽

Mireille Soursac ◽

Robert Farinotti

Keyword(s):

Amino Acids ◽

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

Crown Ether ◽

High Performance ◽

Enantiomeric Separation ◽

Chiral Crown Ether

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Enantioselective multiple heartcut two-dimensional ultra-high-performance liquid chromatography method with a Coreshell chiral stationary phase in the second dimension for analysis of all proteinogenic amino acids in a single run

Journal of Chromatography A ◽

10.1016/j.chroma.2018.05.062 ◽

2018 ◽

Vol 1562 ◽

pp. 69-77 ◽

Author(s):

Ulrich Woiwode ◽

Stefan Neubauer ◽

Wolfgang Lindner ◽

Stephan Buckenmaier ◽

Michael Lämmerhofer

Keyword(s):

Amino Acids ◽

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

Stationary Phase ◽

High Performance ◽

Chiral Stationary Phase ◽

Two Dimensional ◽

Chromatography Method ◽

Liquid Chromatography Method

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A Novel Chiral Stationary Phase for Optical Resolution of Amino Acids and Their Derivatives by Ligand-Exchange High-Performance Liquid Chromatography

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.61.322 ◽

1988 ◽

Vol 61 (1) ◽

pp. 322-324 ◽

Author(s):

Kazuhiko Saigo ◽

Yoichi Yuki ◽

Hiroki Kimoto ◽

Toru Nishida ◽

Masaki Hasegawa

Keyword(s):

Amino Acids ◽

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

Stationary Phase ◽

Ligand Exchange ◽

High Performance ◽

Chiral Stationary Phase ◽

Optical Resolution

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Enantiomeric separation of underivatized α-methyl-α-amino acids by high-performance liquid chromatography

Journal of Chromatography A ◽

10.1016/s0021-9673(01)90670-3 ◽

1985 ◽

Vol 318 ◽

pp. 117-121 ◽

Author(s):

Shulamith Weinstein ◽

Nelu Grinberg

Keyword(s):

Amino Acids ◽

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

High Performance ◽

Enantiomeric Separation

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Enantiomeric separation of nonproteinogenic amino acids by high-performance liquid chromatography

Journal of Chromatography A ◽

10.1016/j.chroma.2012.07.011 ◽

2012 ◽

Vol 1269 ◽

pp. 94-121 ◽

Author(s):

István Ilisz ◽

Anita Aranyi ◽

Zoltán Pataj ◽

Antal Péter

Keyword(s):

Amino Acids ◽

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

High Performance ◽

Enantiomeric Separation

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Enantiomeric Separation of Non-Protein Amino Acids by Chiral Ligand-Exchange High-Performance Liquid Chromatography

Analytical Letters ◽

10.1080/00032719708006430 ◽

1997 ◽

Vol 30 (4) ◽

pp. 867-882 ◽

Author(s):

Toshifumi Miyazawa ◽

Hiroc Minowa ◽

Kiwamu Imagawa ◽

Takashi Yamada

Keyword(s):

Amino Acids ◽

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

Ligand Exchange ◽

High Performance ◽

Enantiomeric Separation ◽

Chiral Ligand ◽

Protein Amino Acids ◽

Chiral Ligand Exchange

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Direct enantiomeric separation of racemic flavanones by high-performance liquid chromatography using cellulose triacetate as a chiral stationary phase

Journal of Chromatography A ◽

10.1016/s0021-9673(01)83888-7 ◽

1988 ◽

Vol 441 (2) ◽

pp. 417-422 ◽

Author(s):

Martin Krause ◽

Rudolf Galensa

Keyword(s):

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

Stationary Phase ◽

High Performance ◽

Chiral Stationary Phase ◽

Cellulose Triacetate ◽

Enantiomeric Separation

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Enantiomeric resolution of derivatized dl-amino acids by high-performance liquid chromatography using a β-cyclodextrin chiral stationary phase: A comparison between derivatization labels

Journal of Chromatography A ◽

10.1016/0021-9673(95)00498-x ◽

1995 ◽

Vol 710 (2) ◽

pp. 287-295 ◽

Author(s):

Andreas M. Rizzi ◽

Sabine Cladrowa-Runge ◽

Helén Jonsson ◽

Susanne Osla

Keyword(s):

Amino Acids ◽

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

Stationary Phase ◽

High Performance ◽

Chiral Stationary Phase ◽

Enantiomeric Resolution

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Enantiomeric separation of azelnidipine by high performance liquid chromatography with chiral stationary phase

Chinese Journal of Chromatography ◽

10.3724/sp.j.1123.2012.00215 ◽

2010 ◽

Vol 28 (2) ◽

pp. 215-217 ◽

Author(s):

Kai ZHANG ◽

Na XUE ◽

Lin LI ◽

Fan LI ◽

Yumin DU

Keyword(s):

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

Stationary Phase ◽

High Performance ◽

Chiral Stationary Phase ◽

Enantiomeric Separation

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Enantiomeric Separation and Detection of 2-Arylpropionic Acids Derivatized with [(N,N-Dimethylamino)sulfonyl]benzofurazan Reagents on a Modified Cellulose Stationary Phase by High-Performance Liquid Chromatography

Analytical Chemistry ◽

10.1021/ac961105g ◽

1997 ◽

Vol 69 (9) ◽

pp. 1793-1799 ◽

Author(s):

Takeshi Fukushima ◽

Tomofumi Santa ◽

Hiroshi Homma ◽

Salma M. Al-kindy ◽

Kazuhiro Imai

Keyword(s):

High Performance Liquid Chromatography ◽

Liquid Chromatography ◽

Stationary Phase ◽

High Performance ◽

Enantiomeric Separation ◽

Modified Cellulose

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