TECHNICAL LIBRARY
Chiral Technologies’ stationary phases are applied to enantioseparations of a great variety of chiral compounds. Technical Library contains Publications in a number of scientific journals. Publications are grouped by use of specific stationary phases. Technical Library also contains Application Notes and Presentations given at conferences and trade shows.
Ref from: chiraltech.com/technical-library/#publications
PUBLICATIONS
Polysaccharide Chiral Stationary Phases
Poly(butylene terephthalate) based novel achiral stationary phase investigated under supercritical fluid chromatography conditions, K. Nagai, T. Shibata, S. Shinkura, A. Ohnishi, J. Sep. Sci., (2018)
Development of an HPLC method for the simultaneous determination of chiral impurities and assay of (S)-Clopidogrel using a cellulose-based chiral stationary phase in methanol/water mode, R. Ferretti, L. Zanitti, R. Cirilli, J. Sep. Sci., (2017)
A chromatographic study on the exceptional chiral recognition of 2-(benzylsulfinyl) benzamide by an immobilized-type chiral stationary phase based on cellulose tris(3,5-dichlorophenylcarbamate), S. Carradori, D. Secci, C. Faggi, R. Cirilli, J. Chromatogr. A, 1531, (2018), 151-156
Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition, T. Shibata, S. Shinkura, A. Ohnishi, K. Ueda, Molecules, 22, (2017), 38
Enantioselective reaction monitoring utilizing two-dimensional heart-cut liquid chromatography on an integrated microfluidic chip, C. Lotter, E. Poehler, J. Heiland, L. Mauritz, D. Belder, Lab Chip, 16, (2016), 4648–4652
Bioanalytical method for the simultaneous determination of d- and l-serine in human plasma by LC/MS/MS, H. Sugimoto, M. Kakehi, F. Jinno, Anal. Biochem.,487 (2015) 38-44
Multigram Synthesis and in Vivo Efficacy Studies of a Novel Multitarget Anti-Alzheimer’s Compound,
I. Sola, E. Viayna, T. Gomez, C. Galdeano, M. Cassina, P. Camps, M. Romeo, L. Diomede,
M. Salmona, P. Franco, M. Schaeffer, D. Colantuono, D. Robin, D. Brunner, N. Taub, B. Hutter-Paier, D. Muñoz-Torrero, Molecules, 20 (2015) 4492-4515
On the method development of immobilized polysaccharide chiral stationary phases in supercritical fluid chromatography using an extended range of modifiers, J. Lee, J.T. Lee, W.L. Watts, J. Barendt, T.Q. Yan, Y. Huang, F. Riley, M. Hardink, J. Bradow, P. Franco, J. Chromatogr. A (2014)
Polysaccharide Derivatives for Chromatographic Separation of Enantiomers, Y. Okamoto, E. Yashima, Angew. Chem. Int. Ed., 37 (1998) 1020–1043
Enantioselective chromatography as a powerful alternative for the preparation of drug enantiomers, E. R. Francotte, J. Chromatogr. A, 906 (2001) 379-397
Reversed-phase liquid chromatographic separation of enantiomers on polysaccharide type chiral stationary phases, K. Tachibana, A. Ohnishi, J. Chromatogr. A, 906 (2001) 127-154
Polysaccharide-based chiral stationary phases for high-performance liquid chromatographic enantioseparation, E. Yashima, J. Chromatogr. A, 906 (2001) 105-125
Chromatography as a Separation Tool for the Preparative Resolution of Racemic Compounds, E. R. Francotte, ChemInform, 28 (1997)
Solvent versatility of immobilized 3,5-dimethylphenylcarbamate of amylose in enantiomeric separations by HPLC, T. Zhang, C. Kientzy, P. Franco, A. Ohnishi, Y. Kagamihara, H. Kurosawa, J. Chromatogr. A, 1075 (2005) 65-75
Cellulose tris(3,5-dichlorophenylcarbamate) immobilised on silica: A novel chiral stationary phase for resolution of enantiomers, T. Zhang, D. Nguyen, P. Franco, Y. Isobe, T. Michishita, T. Murakami, J. Pharm. Biochem. Anal., 46 (2008) 882-891
Cellulose 3,5-dimethylphenylcarbamate immobilized on silica: A new chiral stationary phase for the analysis of enantiomers, T. Zhang, D. Nguyen, P. Franco, T. Murakami, A. Ohnishi, H. Kurosawa, Anal. Chim. Acta, 557 (2006) 221-228
Optimization of the chiral separation of a Ca-sensitizing drug on an immobilized polysaccharide-based chiral stationary phase: Case study with a preparative perspective, T. Zhang, M. Schaeffer, P. Franco, J. Chromatogr. A, 1083 (2005) 96-101
Enantiomer resolution screening strategy using multiple immobilised polysaccharide-based chiral stationary phases, T. Zhang, D. Nguyen, P. Franco, J. Chromatogr. A, 1191 (2008) 214-222
Complementary enantiorecognition patterns and specific method optimization aspects on immobilized polysaccharide-derived chiral stationary phases, T. Zhang, P. Franco, D. Nguyen. R. Hamasaki, S. Miyamoto, A. Ohnishi. T. Murakamo, J. Chromatogr. A, 1269 (2012) 178–188
Reversed-phase screening strategies for liquid chromatography on polysaccharide-derived chiral stationary phases, T. Zhang, D. Nguyen, P. Franco, J. Chromatogr. A, 1217 (2010) 1048–1055
Practical access to the proline analogs (S,S,S)- and (R,R,R)-2-ethyloctahydroindole-carboxylic acids by HPLC enantioseparation, F. J. Sayago, M. J. Pueyo, M. I. Calaza, A. I. Jimenez. C. Cativiela, Chirality, 23, (2011) 507–513
Organocatalytic Aryl-Aryl Bond-Formation: An Atroposelective [3,3]-Rearrangement Approach to BINAM Derivatives, G-Q. Li, H. Gao, C. Keene, M. Devonas, D. H. Ess, L. Kurti, Am. Chem. Soc., 135 (2013) 7414–7417
Common approaches for efficient method development with immobilised polysaccharide-derived chiral stationary phases, P. Franco, T. Zhang, J. Chromatogr. B, 875 (2008) 48
Novel stereoselective synthesis and chromatographic evaluation of E-guggulsterone, A. Gioiello, R. Sardella, E. Rosatello, B. Sadeghpour, B. Natalini, R. Pellicciari, Steroids, 77 (2012) 250–254
Preparative enantioseparations using supercritical fluid chromatography, L. Miller, J. Chromatogr. A, 1250 (2012) 250-255
Evaluation of non-traditional modifiers for analytical and preparative enantioseparations using supercritical fluid chromatography, L. Miller, J. Chromatogr. A, 1256 (2012) 261-266
High-performance liquid chromatographic separation of enantiomers and diastereomers of 2-methylcyclohexanone thiosemicarbazone, and determination of absolute configuration and configurational stability, R. Cirilli, R. Ferretti, F. La Torre, D. Secci, A. Bolasco, S. Carradoni, M. Pierini, J. Chromatogr. A, 1172 (2007) 160-169
High-performance liquid chromatography enantioseparation of proton pump inhibitors using the immobilized amylose-based CHIRALPAK IA chiral stationary phase in normal-phase, polar organic and reversed-phase conditions, R. Cirilli, R. Ferretti, B. Gallinella, E. De Santis, L. Zanitti, F. La Torre, J. Chromatogr. A, 1177 (2008) 105-113
Analytical and semipreparative high performance liquid chromatography enantioseparation of new substituted 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)-pyrazoles on polysaccharide-based chiral stationary phases in normal-phase, polar organic and reversed-phase conditions, R. Cirilli, A. Simonelli, R. Ferretti, A. Bolasco, P. Chimenti, D. Secci, E. Maccioni, F. La Torre, J. Chromatogr. A, 1101 (2006) 198-203
Direct HPLC enantioseparation of chiral aptazepine derivatives on coated and immobilized polysaccharide-based chiral stationary phases, R. Cirilli, V. Orlando, R. Ferretti, L. Turchetto, R. Silvestri, G. De Martino, F. La Torre, Chirality 18, (2006) 621-632
Development and validation of an enantioselective and chemoselective HPLC method using a CHIRALPAK IA column to simultaneously quantify (R)-(+)- and (S)-(−)-lansoprazole enantiomers and related impurities, R. Cirilli, R. Ferretti, B. Gallinella, L. Turchetto, L. Zanitti, F. La Torre, J. Pharm. Biochem. Anal., 50, (2009) 9-14
Direct high-performance liquid chromatography enantioseparation of terazosin on an immobilised polysaccharide-based chiral stationary phase under polar organic and reversed-phase conditions, R. Ferretti, B. Gallinella, F. La Torre, L. Zanitti, L. Turchetto, A. Mosca, R. Cerilli, J. Chromatogr. A, 1216 (2009) 5385-5390
Synthesis and chromatographic enantioresolution of anti-HIV quinolone derivatives, B. Natalini, R. Sardella, S. Massari, F. Ianni, O. Tabarrini, V. Cecchetti, Talanta, 85, (2011) 1392–1397
Evaluation of non-conventional polar modifiers on immobilized chiral stationary phases for improved resolution of enantiomers by supercritical fluid chromatography, J. O. DaSilva, B. Coes, L. Frey, I. Mergelsberg, R. McClain, L. Nogle, C. J. Welch, J. Chromatogr. A, 1328 (2014) 98-103
T. Zhang, P. Franco, Analytical and preparative potential of immobilized polysaccharide-derived chiral stationary phases, in Chiral Separation Techniques – A Practical Approach, third ed., G. Subramanian (Editor), Wiley-VCH, Weinheim, Germany, 2006, 99-134
G.B. Cox, Introduction to preparative chromatography, in Preparative Enantioselective Chromatography, G.B. Cox (Editor), Blackwell Publishing Ltd, Oxford, UK, 2005
P. Franco, T. Zhang, Common screening approaches for efficient analytical method development in LC and SFC on columns packed with immobilized polysaccharide stationary phases, in Chiral Separations, Methods and Protocols, second ed., G. Scriba (Editor), Humana Press, 2013, 113-126
Anion-Exchange Chiral Stationary Phases
Chiral separation of disease biomarkers with 2-hydroxycarboxylic acid structure, C. Calderón, C. Santi, M. Lämmerhofer, J. Sep. Sci., (2017), 1-8
Direct Separation of Pregabalin Enantiomers Using a Zwitterionic Chiral Selector by High Performance Liquid Chromatography Coupled to Mass Spectrometry and Ultraviolet Detection, L. Narayana Chennuru, T. Choppari, R. Prasad Nandula, T. Zhang and P. Franco, Molecules, 21(11), 2016, 1578
Quinine and quinidine derivatives as chiral selectors I. Brush type chiral stationary phases for HPLC based on cinchonan carbamates and their application as chiral anion exchangers, M. Lämmerhofer, W. Lindner, J. Chromatogr. A, 741 (1996) 33-48
Chiral anion exchange-type stationary phases based on cinchonan alkaloids. An effective tool for the separation of enantiomers of chiral acids, M. Lämmerhofer, N. M. Maier, W. Lindner, ChemInform, 29 (1998)
Quinine- versus carbamoylated quinine-based chiral anion exchangers: A comparison regarding enantioselectivity for N-protected amino acids and other chiral acids, A. Mandl, L. Nicoletti, M. Lämmerhofer, W. Lindner, J. Chromatogr. A, 858 (1996) 1-11
Enantioseparation of various amino acid derivatives on a quinine based chiral anion-exchange selector at variable temperature conditions. Influence of structural parameters of the analytes on the apparent retention and enantioseparation characteristics, W. R. Oberleitner, N. M. Maier, W. Lindner, J. Chromatogr. A, 960 (2002) 97-108
Use of evaporative light scattering detector in the detection and quantification of enantiomeric mixtures by HPLC, T. Zhang, D. Nguyen, P. Franco, J. Sep. Sci., 29 (2006) 1517-1524
Kinetic resolution of glyceraldehyde using an aldehyde dehydrogenase from Deinococcus geothermalis DSM 11300 combined with electrochemical cofactor recycling, H. Wulf, M. Perzborn, G. Sievers, F. Scholz, U.T. Bornscheuer, Journal of Molecular Catalysis B: Enzymatic, 74 (2012) 144-150
Enantiomer and topoisomer separation of acidic compounds on anion-exchanger chiral stationary phases by HPLC and SFC, P. Franco, T. Zhang, A. Gargano, M. Mahut, M. Lämmerhofer, W. Lindner, LCGC Europe, 25 (2012) 600-611
Potential of chiral anion-exchangers operated in various subcritical fluid chromatography modes for resolution of chiral acids, R. Pell, W. Lindner, J. Chromatogr. A, 1245 (2012) 175-182
Phosphopeptidomimetic substance libraries from multicomponent reaction: Enantioseparation on quinidine carbamate stationary phase, A. F. G. Gargano, W. Lindner, M. Lämmerhofer, J. Chromatogr. A, 1310 (2013) 56– 65
Simultaneous diastereo- and enantioseparation of farnesoid X receptor (FXR) agonists with a quinine carbamate-based chiral stationary phase, R. Sardella, M. Marinozzi, F. Iammi, A. Lisanti, B. Natalini, Anal. Bioanal. Chem., 405 (2013) 847-862
2-Acyl-dimedones as UV-active protective agents for chiral amino acids: enantiomer separations of the derivatives on chiral anion exchangers, S. Wernisch, F. Bisi, A. S. Cazzato, M. Kohout, W. Lindner, Anal. Bioanal. Chem., 405 (2013) 8011–8026
Zwitterionic Chiral Stationary Phases
Exploring the enantiorecognition mechanism of Cinchona alkaloid-based zwitterionic chiral stationary phases and the basic trans-paroxetine enantiomers, R. Sardella, A. Macchiarulo, F. Urbinati, F. Ianni, A. Carotti, M. Kohout, W. Lindner, A. Peter, I. Ilisz, J. Sep. Sci., (2017)
Liquid chromatographic enantioseparation of limonene-based carbocyclic β-amino acids on zwitterionic Cinchona alkaloid based chiral stationary phases, G. Lajkó, T. Orosz, I. Ugrai, Z. Szakonyi. F. Fülöp, W. Lindner, A. Péter, I. Ilisz, J. Sep. Sci., 40, (2017), 3196-3204
A comparative study for the liquid chromatographic enantioseparation of cyclic β-amino acids and cyclic β-aminohydroxamic acids on Cinchona alkaloid-based zwitterionic chiral stationary phases, A. Bajtai, B. Fekete, M. Palkó, F. Fülöp, W. Lindner, M. Kohout, I. Ilisz, A. Péter, J. Sep. Sci., (2017)
A Comparative Study of Enantioseparations of /N/^α -Fmoc Proteinogenic Amino Acids on /Quinine/-Based Zwitterionic and Anion Exchanger-Type Chiral Stationary Phases under Hydro-Organic Liquid and Subcritical Fluid Chromatographic Conditions, G. Lajkó, N. Grecsó, G. Tóth, F. Fülöp, W. Lindner, A. Péter and I. Ilisz, Molecules , 21 (2016), 1579
Direct Separation of Pregabalin Enantiomers Using a Zwitterionic Chiral Selector by High Performance Liquid Chromatography Coupled to Mass Spectrometry and Ultraviolet Detection, L. Narayana Chennuru, T. Choppari, R. Prasad Nandula, T. Zhang and P. Franco, Molecules, 21 (2016), 1578
Peptide Analysis: Zwitterionic Chiral Ion-Exchangers as Complementary Option to HILIC and to Reversed-Phase Chromatography, T. Zhang, E. Holder, P. Franco, M. Lämmerhofer, A. Sievers-Engler, H. Gerhardt, H. Gross, W. Lindner, LCGC Europe, 29 (2016) 112-128
Method development for the determination of d- and l-isomers of leucine in human plasma by high-performance liquid chromatography tandem mass spectrometry and its application to animal plasma samples, H. Sugimoto, M. Kakehi, F. Jinno, Anal. Bioanal. Chem., 407 (2015) 7889-7898
Unusual temperature-induced retention behavior of constrained β-amino acid enantiomers on the zwitterionic chiral stationary phases ZWIX(+) and ZWIX(-), I. Ilisz, Z. Pataj, Z. Gecse, Z. Szakonyi, F. Fülöp, W. Lindner, A. Péter, Chirality, 26 (2014) 385-93
Structural and temperature effects on enantiomer separations of bicyclo[2.2.2]octane-based 3-amino-2-carboxylic acids on cinchona alkaloid-based zwitterionic chiral stationary phases, I. Ilisz, N. Grecsó, M. Palkó, F. Fülöp, W. Lindner, A. Péter, J. Pharm. Biomed. Anal., 98 (2014) 130-139
Effect of mobile phase composition on the liquid chromatographic enantioseparation of bulky monoterpene-based β-amino acids by applying chiral stationary phases based on Cinchona alkaloid, Z. Pataj, I. Ilisz, Z. Gecse, Z. Szakonyi, F. Fülöp, W. Lindner, A. Péter, J. Sep. Sci., 37 (2014) 1075-1082
Liquid chromatographic enantiomer separation with special focus on zwitterionic chiral ion-exchangers, M. Lämmerhofer, Anal. Bioanal. Chem., 406 (2014) 6095-6103
Simultaneous quantification of mefloquine (+)- and (-)- enantiomers and the carboxy metabolite in dried blood spots by liquid chromatography/tandem mass spectrometry, M. C.K. Geditz, W. Lindner, M. Lämmerhofer, G. Heinkele, R. Kerb, M. Ramharter, M. Schwab, U. Hofmann, J. Chromatogr. B, 968 (2014) 32–39
Direct high-performance liquid chromatographic enantioseparation of secondary amino acids on Cinchona alkaloid-based chiral zwitterionic stationary phases. Unusual temperature behavior, I. Ilisz, Z. Gecsea, Z. Pataja, F. Fülöpb, G. Tóthc, W. Lindner, A. Péter, J. Chromatogr. A, 1363 (2014) 169-177
Direct enantioseparation of underivatized aliphatic 3-hydroxyalkanoic acids with a quinine-based zwitterionic chiral stationary phase, F. Ianni, Z. Pataj, H. Gross, R. Sardella, B. Natalini, W. Lindner, M. Lämmerhofer, J. Chromatogr. A, 1363 (2014) 101-108
Zwitterionic chiral stationary phases based in cinchona and chiral sulfonic acids for the direct stereoselective separation of amino acids and other amphoteric compounds, T. Zhang, E. Holder, P. Franco, W. Lindner, J. Sep. Sci., 37 (2014) 1237-1247
Method development and optimization on cinchona and chiral sulfonic acid-based zwitterionic stationary phases for enantiomer separations of free amino acids by high-performance liquid chromatography, T. Zhang, E. Holder, P. Franco, W. Lindner, J. Chromatogr. A, 1363 (2014) 191-199
Direct high-performance liquid chromatographic enantioseparation of free α-, β- and γ-aminophosphonic acids employing cinchona-based chiral zwitterionic ion exchangers, A. F. G. Gargano, M. Kohout, P. Macikova, M. Lämmerhofer, W. Lindner, Anal. Bioanal. Chem., 405 (2013) 8027–8038
Enantioselective recognition at mesoporous chiral metal surfaces, C. Wattanakit, Y. Bon Saint Côme, V. Lapeyre, P. A. Bopp, M. Heim, S. Yadnum, S. Nokbin, C. Warakulwit, J. Limtrakul, A. Kuhn, Nat. Commun., 5, 3325 (2014)
Stationary phase-related Investigations of quinine-based zwitterionic chiral stationary phases operated in anion-, cation-, and zwitterion-exchange modes, C. Hoffmann, R. Reischl, N. M. Maier, M. Lämmerhofer, W. Lindner, J. Chromatogr. A, 1216 (2009) 1147-1156
Investigations of mobile phase contributions to enantioselective anion and zwitterion exchange modes on quinine-based zwitterionic chiral stationary phases, C. Hoffmann, R. Reischl, N. M. Maier, M. Lämmerhofer, W. Lindner. J. Chromatogr. A, 1216 (2009) 1157-1166
Synergistic effects on enantioselectivity of novel zwitterionic chiral stationary phases for separations of chiral acids, bases, and amino acids by HPLC, C. Hoffmann, R. Pell, M. Lämmerhofer, W. Lindner, Anal. Chem., 80 (2008) 8780-8789
Increments to chiral recognition facilitating enantiomer separations of chiral acids, bases and ampholytes using cinchona-based zwitterion exchanger chiral stationary phases, S. Wernisch, R. Pell, W. Lindner, J. Sep. Sci., 3 (2012) 1560-1572
Diastereoselective discrimination of lysine-alanine peptides by zwitterionic cinchona alkaloid-based chiral selectors using electrospray ionization mass spectrometry, J. M. Bobbitt, L. Li, D. D. Carlton, M. Yasin, S. Bhawal, F. W. Foss, S. Wernisch, R. Pell, W. Lindner, K. A. Schug, J. Chromatogr. A, 1269 (2012) 308-315
Versatility of cinchona-based zwitterionic chiral stationary phases: Enantiomer and diastereomer separations of non-protected oligopeptides utilizing a multi-modal chiral recognition mechanism, S. Wernisch, W. Lindner, J. Chromatogr. A, 1269 (2012) 297-307
Mechanistic investigations of cinchona alkaloid-based zwitterionic chiral stationary phases, R. Pell, S. Sic, W. Lindner, J. Chromatogr. A, 1269 (2012) 287-296
Enantioseparation of 6-aminoquinolyl-n-hydroxysuccinimidyl carbamate tagged amino acids and other zwitterionic compounds on cinchona-based chiral stationary phases, R. Hellinger, J. Horak, W. Lindner, Anal. Bioanal. Chem., 405 (2013) 8105-8120
Application of cinchona-sulfonate-based chiral zwitterionic ion exchangers for the separation of proline-containing dipeptide rotamers and determination of on-column isomerization parameters from dynamic elution profiles, S. Wernisch, O. Trapp, W. Lindner, Anal.Chim Acta, 795 (2013) 88-98
Enantioseparation of β2-amino acids on cinchona alkaloid-based zwitterionic chiral stationary phases. Structural and temperature effects, I. Ilisz, N. Grecsó, A. Aranyi, P. Suchotin, D. Tymecka, B. Wilenska, A. Misicka, F. Fülöp, W. Lindner, A. Péter, J. Chromatogr. A, 1334 (2014) 44-54
Automated and simultaneous two-dimensional micro-high-performance liquid chromatographic determination of proline and hydroxyproline enantiomers in mammals, Y. Tojo, K. Hamase, M. Nakata, A. Morikawa, M. Mita, Y. Ashida, W. Lindner, K. Zaitsu, J. Chromatogr. B, 875 (2008) 174-179
Simultaneous determination of d-aspartic acid and d-glutamic acid in rat tissues and physiological fluids using a multi-loop two-dimensional HPLC procedure, H. Han, Y. Miyoshi, K. Ueno, C. Okamura, Y. Tojo, M. Mita, W. Lindner, K. Zaitsu, K. Hamase, J. Chromatogr. B, 879 (2011) 3196-3202
Enantioselective two-dimensional high-performance liquid chromatographic determination of n-methyl-d-aspartic acid and its analogues in mammals and bivalves, R. Koga, Y. Miyoshi, E. Negishi, T. Kaneko, M. Mita, W. Lindner, K. Hamase, J. Chromatogr. A, 1269 (2012) 255-261
Protein-Based Chiral Stationary Phases
New approaches of LC-MS compatible method development on α1-acid glycoprotein-based stationary phase for resolution of enantiomers by HPLC, T. Michishita, P. Franco, T. Zhang, J. Sep. Sci., 3627 (2010) 23-24
Trace analysis of fluoxetine and its metabolite norfluoxetine. Part I: Development of a chiral liquid chromatography – tandem mass spectrometry method for wastewater samples, V. K. H. Barclay, N. L. Tyrefors, I. M. Johansson, C. E. Pettersson, J. Chromatogr. A, 1218 (2011) 5587-5596
Enantiomeric analysis of drugs of abuse in wastewater by chiral liquid chromatography coupled with tandem mass spectrometry, B. Kasprzyk-Hordern, V. V. R. Kondakal, D. R. Baker, J. Chromatogr. A, 1217 (2010) 4575-4586
APPLICATION NOTES
Separation of Naproxen using the new immobilized column – CHIRALPAK IH
Introducing the First sub-2 Micron Chiral Columns From Daicel
Separation of Methyclothiazide Using New Immobilized Column – CHIRALPAK IG
High-Speed SFC Enantiomeric Separation Using the Optimal Daicel SFC Chiral Columns
Separation of enantiomers and conformers of Tofisopam using Daicel immobilized polysaccharide-derived chiral columns using the Agilent 1260 Infinity Analytical SFC System, T. Zhang, N. Nguyen, P. Franco, M. Vollmer, Application Note (Agilent, 2011)
Enantiomer separation of non-steroidal anti-inflammatory drugs, T. Zhang, N. Nguyen, P. Franco, M. Vollmer, Application Note (Agilent, 2011)
Enantiomer separation of acidic compounds using Daicel CHIRALPAK QN-AX and QD-AX columns and the Agilent 1260 Infinity Analytical SFC System, T. Zhang, N. Nguyen, P. Franco, M. Vollmer, Application Note (Agilent, 2011)
Pressure Stability of Wide-Pore Diameter Chiral Chromatography Columns
Two Novel Polysaccharide-Based Chiral Stationary Phases: CHIRALPAK® AY-H and CHIRALCEL® OZ-H
Reversed-Phase Enantioselective Chromatography with New 3-micron Chiral Stationary Phases
Fast Enantioselective Chromatography with 3-micron Particles
Daicel 3-micron CHIRALPAK® and CHIRALCEL® Analytical Columns
CHIRALPAK® IC – An Immobilized Polysaccharide Chiral Stationary Phase with a Unique Chiral Selector
Chiral Separations on a New Commercially Available Immobilized Cellulose Column, CHIRALPAK® IB
Enantioselective Reversed-Phase Chromatography with Protein-Based Columns
SMB Process Development and Optimization Using Immobilized Chiral Stationary Phases: Chiral Separation of 1-Methyl-1-Phenylsuccinimide Using a THF Based Mobile Phase
PRESENTATIONS
Multimilligram Stack Injection Chiral Separation of MDMA – HPLC 2014, New Orleans, LA
Advances in Method Development for Preparative Chiral Chromatography – Prep 2014, Boston, MA
Preparative Chiral Chromatography – SPICA 2012, Brussels, Belgium
Chirality in the Natural Sciences – AgroChemical Conference 2012, Cambridge, UK
Chirality. Asymmetric, Enzymatic…Is there a better way? – ChemOutsourcing 2012, Long Branch, NJ
New 3-Micron Polysaccharide-based Chiral Columns for Fast HPLC and SFC – PittCon 2009, Chicago, IL
GiMiTEC.info
