Hage DS (2001) Chromatographic and electrophoretic studies of protein binding to chiral solutes. J
Chromatogr A 906(1–2):459–481
Haginaka J, Kanasugi N (1997) Enantioselectivity of bovine serum albumin-bonded columns
produced with isolated protein fragments. II. Characterization of protein fragments and chiral
binding sites. J Chromatogr A 769(2):215–223
Han J, Kitagawa O, Wzorek A, Klika KD, Soloshonok VA (2018) The self-disproportionation of
enantiomers (SDE): a menace or an opportunity? Chem Sci 9(7):1718–1739
Hare PE, Gil-Av E (1979) Separation of D and L amino acids by liquid chromatography: use of
chiral eluants. Science 204(4398):1226–1228
Hayamizu T, Kudoh S, Nakamura H (1998) Methylated Nepsilon-dansyl-L-lysine as a fluorogenic
reagent for the chiral separation of carboxylic acids. J Chromatogr B Biomed Sci Appl 710
(1–2):211–218
Hegade RS, De Beer M, Lynen F (2017) Chiral stationary phase optimized selectivity liquid
chromatography: A strategy for the separation of chiral isomers. J Chromatogr A 1515:109–117
Hendrickx A, Mangelings D, Chankvetadze B, Vander Heyden Y (2011) Updating a chiral
separation strategy for non-acidic drugs with capillary electrochromatography applicable for
both chlorinated and non-chlorinated polysaccharide selectors. Electrophoresis 32
(19):2718–2726
Hesse G, Nagel R (1973) Eine vollständiger Racemattrennung durch Elutionschromatographie an
Cellulose-tri-acetat. Chromatographia 6(6):277–280
Hinze WL, William RWJ, Fu ZS, Suzuki Y, Quina FH (1990) Novel chiral separation techniques
based on surfactants. Coll Surf 48:79–94
Hou J, Zhou Z, Chen L, Ou Q (1997) [Brush-type chiral stationary phase for chiral resolution in
high performance liquid chromatography]. Se Pu 15(3):206–211
Howard JW, Kay RG, Pleasance S, Creaser CS (2012) UHPLC for the separation of proteins and
peptides. Bioanalysis 4(24):2971–2988
Huang G, Ou J, Zhang X, Ji Y, Peng X, Zou H (2014) Synthesis of novel perphenylcarbamated
beta-cyclodextrin based chiral stationary phases via thiol-ene click chemistry. Electrophoresis
35(19):2752–2758
Huang XY, Pei D, Liu JF, Di DL (2018a) A review on chiral separation by counter-current
chromatography: Development, applications and future outlook. J Chromatogr A 1531:1–12
Huang XY, Quan KJ, Pei D, Liu JF, Di DL (2018b) The development of biphasic chiral recognition
in chiral separation. Chirality. https://doi.org/10.1002/chir.22975
Hühnerfuss H, Shah MA (2009) Enantioselective chromatography - a powerful tool for the
discrimination of biotic and abiotic processes of chiral environmental pollutants. J Chromatogr
A 1216/13:481–502
Hui F, Ekborg-Ott KH, Armstrong DW (2001) High-performance liquid chromatographic and
capillary electrophoretic enantioseparation of plant growth regulators and related indole compounds using macrocyclic antibiotics as chiral selectors. J Chromatogr A 906(1–2):91–103
Hyun MH (2018) Liquid chromatographic ligand-exchange chiral stationary phases based on amino
alcohols. J Chromatogr A 1557:28–42
Ianni F, Sardella R, Carotti A, Natalini B, Lindner W, Lammerhofer M (2016) Quinine-based
zwitterionic chiral stationary phase as a complementary tool for peptide analysis: mobile phase
effects on enantio- and stereoselectivity of underivatized oligopeptides. Chirality 28(1):5–16
Ilisz I, Bajtai A, Lindner W, Peter A (2018) Liquid chromatographic enantiomer separations
applying chiral ion-exchangers based on Cinchona alkaloids. J Pharm Biomed Anal
159:127–152
Iorio MA, Tomassini L, Mattson MV, George C, Jacobson AE (1991) Synthesis, stereochemistry,
and biological activity of the 1-(1-phenyl-2-methylcyclohexyl)piperidines and the 1-(1-phenyl4-methylcyclohexyl)piperidines. Absolute configuration of the potent trans-(-)-1-(1-phenyl-2methylcyclohexyl)piperidine. J Med Chem 34(8):2615–2623
References
53
Chromatogr A 906(1–2):459–481
Haginaka J, Kanasugi N (1997) Enantioselectivity of bovine serum albumin-bonded columns
produced with isolated protein fragments. II. Characterization of protein fragments and chiral
binding sites. J Chromatogr A 769(2):215–223
Han J, Kitagawa O, Wzorek A, Klika KD, Soloshonok VA (2018) The self-disproportionation of
enantiomers (SDE): a menace or an opportunity? Chem Sci 9(7):1718–1739
Hare PE, Gil-Av E (1979) Separation of D and L amino acids by liquid chromatography: use of
chiral eluants. Science 204(4398):1226–1228
Hayamizu T, Kudoh S, Nakamura H (1998) Methylated Nepsilon-dansyl-L-lysine as a fluorogenic
reagent for the chiral separation of carboxylic acids. J Chromatogr B Biomed Sci Appl 710
(1–2):211–218
Hegade RS, De Beer M, Lynen F (2017) Chiral stationary phase optimized selectivity liquid
chromatography: A strategy for the separation of chiral isomers. J Chromatogr A 1515:109–117
Hendrickx A, Mangelings D, Chankvetadze B, Vander Heyden Y (2011) Updating a chiral
separation strategy for non-acidic drugs with capillary electrochromatography applicable for
both chlorinated and non-chlorinated polysaccharide selectors. Electrophoresis 32
(19):2718–2726
Hesse G, Nagel R (1973) Eine vollständiger Racemattrennung durch Elutionschromatographie an
Cellulose-tri-acetat. Chromatographia 6(6):277–280
Hinze WL, William RWJ, Fu ZS, Suzuki Y, Quina FH (1990) Novel chiral separation techniques
based on surfactants. Coll Surf 48:79–94
Hou J, Zhou Z, Chen L, Ou Q (1997) [Brush-type chiral stationary phase for chiral resolution in
high performance liquid chromatography]. Se Pu 15(3):206–211
Howard JW, Kay RG, Pleasance S, Creaser CS (2012) UHPLC for the separation of proteins and
peptides. Bioanalysis 4(24):2971–2988
Huang G, Ou J, Zhang X, Ji Y, Peng X, Zou H (2014) Synthesis of novel perphenylcarbamated
beta-cyclodextrin based chiral stationary phases via thiol-ene click chemistry. Electrophoresis
35(19):2752–2758
Huang XY, Pei D, Liu JF, Di DL (2018a) A review on chiral separation by counter-current
chromatography: Development, applications and future outlook. J Chromatogr A 1531:1–12
Huang XY, Quan KJ, Pei D, Liu JF, Di DL (2018b) The development of biphasic chiral recognition
in chiral separation. Chirality. https://doi.org/10.1002/chir.22975
Hühnerfuss H, Shah MA (2009) Enantioselective chromatography - a powerful tool for the
discrimination of biotic and abiotic processes of chiral environmental pollutants. J Chromatogr
A 1216/13:481–502
Hui F, Ekborg-Ott KH, Armstrong DW (2001) High-performance liquid chromatographic and
capillary electrophoretic enantioseparation of plant growth regulators and related indole compounds using macrocyclic antibiotics as chiral selectors. J Chromatogr A 906(1–2):91–103
Hyun MH (2018) Liquid chromatographic ligand-exchange chiral stationary phases based on amino
alcohols. J Chromatogr A 1557:28–42
Ianni F, Sardella R, Carotti A, Natalini B, Lindner W, Lammerhofer M (2016) Quinine-based
zwitterionic chiral stationary phase as a complementary tool for peptide analysis: mobile phase
effects on enantio- and stereoselectivity of underivatized oligopeptides. Chirality 28(1):5–16
Ilisz I, Bajtai A, Lindner W, Peter A (2018) Liquid chromatographic enantiomer separations
applying chiral ion-exchangers based on Cinchona alkaloids. J Pharm Biomed Anal
159:127–152
Iorio MA, Tomassini L, Mattson MV, George C, Jacobson AE (1991) Synthesis, stereochemistry,
and biological activity of the 1-(1-phenyl-2-methylcyclohexyl)piperidines and the 1-(1-phenyl4-methylcyclohexyl)piperidines. Absolute configuration of the potent trans-(-)-1-(1-phenyl-2methylcyclohexyl)piperidine. J Med Chem 34(8):2615–2623
References
53