Berthod A (2009) Chiral recognition mechanisms with macrocyclic glycopeptide selectors. Chirality 21(1):167–175
Bhushan R, Martens J (1998) Resolution of enantiomers of ibuprofen by liquid chromatography: a
review. Biomed Chromatogr 12(6):309–316
Bickel CL, Peaslee Jr AT (1948) Melting point curves of optical isomers. J Am Chem Soc 70
(5):1790
Bicker W, Lammerhofer M, Lindner W (2004) Direct high-performance liquid chromatographic
method for enantioselective and diastereoselective determination of selected pyrethroic acids. J
Chromatogr A 1035(1):37–46
Bielejewska A, Duszczyk K, Zukowski J (2005) Effect of (+) or (-) camphorsulfonic acid additives
to the mobile phase on enantioseparations of some basic drugs on a Chiralcel OD column. J
Chromatogr A 1083(1–2):133–140
Blankenburg S, Schmidt WG (2007) Long-range chiral recognition due to substrate locking and
substrate-adsorbate charge transfer. Phys Rev Lett 99(19):196107
Bunton BM, Walker TA (1995) Chiral separation of MDL 73,005EF enantiomers using an alpha
1-acid glycoprotein column. J Chromatogr A 699(1–2):389–394
Burden RS, Deas AH, Clark T (1987) Separation of enantiomers of fungicidal and plant growth
regulatory triazole alcohols using chiral derivatisation and capillary gas chromatography. J
Chromatogr 391(1):273–279
Caballo C, Sicilia MD, Rubio S (2013) Stereoselective quantitation of mecoprop and dichlorprop in
natural waters by supramolecular solvent-based microextraction, chiral liquid chromatography
and tandem mass spectrometry. Anal Chim Acta 761:102–108
Calderon C, Lammerhofer M (2017) Chiral separation of short chain aliphatic hydroxycarboxylic
acids on cinchonan carbamate-based weak chiral anion exchangers and zwitterionic chiral ion
exchangers. J Chromatogr A 1487:194–200
Camacho-Munoz D, Kasprzyk-Hordern B, Thomas KV (2016) Enantioselective simultaneous
analysis of selected pharmaceuticals in environmental samples by ultrahigh performance supercritical fluid based chromatography tandem mass spectrometry. Anal Chim Acta 934:239–251
Camilleri P (1997) Chiral surfactants in micellar electrokinetic capillary chromatography. Electrophoresis 18(12-13):2322–2330
Cappiello A (2007) Advances in LC-MS instrumentation. Elsevier, Boston, MA
Cappiello A, Palma P (2018) Advances in the use of liquid chromatography mass spectrometry
(LC-MS) : instrumentation developments and application. Elsevier, Amsterdam
Carrasco-Correa EJ, Simo-Alfonso EF, Ramis-Ramos G, Herero-Martinez JM (2017) Application
of organic monolithic materials to enantioseparation in capillary separation techniques. Curr
Med Chem 24(8):781–795
Cavazzini A, Pasti L, Massi A, Marchetti N, Dondi F (2011) Recent applications in chiral high
performance liquid chromatography: a review. Anal Chim Acta 706(2):205–222
Charles R, Beitler U, Feibush B, Gil-Av E (1975) Separation of enantiomers on packed columns
containing optically active diamide phases. J Chromatogr 112:121–133
Chen J, Shi H (2017) [Research progress of bonded chiral stationary phases]. Se Pu 35
(12):1229–1239
Cho HS, Choi HJ, Hyun MH (2009) Preparation of a new crown ether-based chiral stationary phase
containing thioester linkage for the liquid chromatographic separation of enantiomers. J
Chromatogr A 1216(44):7446–7449
Cielecka-Piontek J, Zalewski P, Jelinska A, Garbacki P (2013) UHPLC: the greening face of liquid
chromatography. Chromatographia 76:1429–1437
Ciogli A, Ismail OH, Mazzoccanti G, Villani C, Gasparrini F (2018) Enantioselective ultra high
performance liquid and supercritical fluid chromatography: The race to the shortest chromatogram. J Sep Sci 41(6):1307–1318
Cirilli R, Orlando V, Ferretti R, Turchetto L, Silvestri R, De Martino G, La Torre F (2006) Direct
HPLC enantioseparation of chiral aptazepine derivatives on coated and immobilized
polysaccharide-based chiral stationary phases. Chirality 18(8):621–632
50
3 Enantiomer-Selective High- and Ultra- High-Performance Liquid Chromatography
Bhushan R, Martens J (1998) Resolution of enantiomers of ibuprofen by liquid chromatography: a
review. Biomed Chromatogr 12(6):309–316
Bickel CL, Peaslee Jr AT (1948) Melting point curves of optical isomers. J Am Chem Soc 70
(5):1790
Bicker W, Lammerhofer M, Lindner W (2004) Direct high-performance liquid chromatographic
method for enantioselective and diastereoselective determination of selected pyrethroic acids. J
Chromatogr A 1035(1):37–46
Bielejewska A, Duszczyk K, Zukowski J (2005) Effect of (+) or (-) camphorsulfonic acid additives
to the mobile phase on enantioseparations of some basic drugs on a Chiralcel OD column. J
Chromatogr A 1083(1–2):133–140
Blankenburg S, Schmidt WG (2007) Long-range chiral recognition due to substrate locking and
substrate-adsorbate charge transfer. Phys Rev Lett 99(19):196107
Bunton BM, Walker TA (1995) Chiral separation of MDL 73,005EF enantiomers using an alpha
1-acid glycoprotein column. J Chromatogr A 699(1–2):389–394
Burden RS, Deas AH, Clark T (1987) Separation of enantiomers of fungicidal and plant growth
regulatory triazole alcohols using chiral derivatisation and capillary gas chromatography. J
Chromatogr 391(1):273–279
Caballo C, Sicilia MD, Rubio S (2013) Stereoselective quantitation of mecoprop and dichlorprop in
natural waters by supramolecular solvent-based microextraction, chiral liquid chromatography
and tandem mass spectrometry. Anal Chim Acta 761:102–108
Calderon C, Lammerhofer M (2017) Chiral separation of short chain aliphatic hydroxycarboxylic
acids on cinchonan carbamate-based weak chiral anion exchangers and zwitterionic chiral ion
exchangers. J Chromatogr A 1487:194–200
Camacho-Munoz D, Kasprzyk-Hordern B, Thomas KV (2016) Enantioselective simultaneous
analysis of selected pharmaceuticals in environmental samples by ultrahigh performance supercritical fluid based chromatography tandem mass spectrometry. Anal Chim Acta 934:239–251
Camilleri P (1997) Chiral surfactants in micellar electrokinetic capillary chromatography. Electrophoresis 18(12-13):2322–2330
Cappiello A (2007) Advances in LC-MS instrumentation. Elsevier, Boston, MA
Cappiello A, Palma P (2018) Advances in the use of liquid chromatography mass spectrometry
(LC-MS) : instrumentation developments and application. Elsevier, Amsterdam
Carrasco-Correa EJ, Simo-Alfonso EF, Ramis-Ramos G, Herero-Martinez JM (2017) Application
of organic monolithic materials to enantioseparation in capillary separation techniques. Curr
Med Chem 24(8):781–795
Cavazzini A, Pasti L, Massi A, Marchetti N, Dondi F (2011) Recent applications in chiral high
performance liquid chromatography: a review. Anal Chim Acta 706(2):205–222
Charles R, Beitler U, Feibush B, Gil-Av E (1975) Separation of enantiomers on packed columns
containing optically active diamide phases. J Chromatogr 112:121–133
Chen J, Shi H (2017) [Research progress of bonded chiral stationary phases]. Se Pu 35
(12):1229–1239
Cho HS, Choi HJ, Hyun MH (2009) Preparation of a new crown ether-based chiral stationary phase
containing thioester linkage for the liquid chromatographic separation of enantiomers. J
Chromatogr A 1216(44):7446–7449
Cielecka-Piontek J, Zalewski P, Jelinska A, Garbacki P (2013) UHPLC: the greening face of liquid
chromatography. Chromatographia 76:1429–1437
Ciogli A, Ismail OH, Mazzoccanti G, Villani C, Gasparrini F (2018) Enantioselective ultra high
performance liquid and supercritical fluid chromatography: The race to the shortest chromatogram. J Sep Sci 41(6):1307–1318
Cirilli R, Orlando V, Ferretti R, Turchetto L, Silvestri R, De Martino G, La Torre F (2006) Direct
HPLC enantioseparation of chiral aptazepine derivatives on coated and immobilized
polysaccharide-based chiral stationary phases. Chirality 18(8):621–632
50
3 Enantiomer-Selective High- and Ultra- High-Performance Liquid Chromatography