Negi S, Dhanasekaran M, Hirata T, Urata H, Sugiura Y (2006) Biomolecular mirror-image
recognition: reciprocal chiral-specific DNA binding of synthetic enantiomers of zinc finger
domain from GAGA factor. Chirality 18(4):254–258
Nemeth T, Levai S, Fodi T, Kupai J, Turos G, Toth T, Huszthy P, Balogh GT (2015) A novel
method for the preparation of a chiral stationary phase containing an enantiopure acridino-18crown-6 ether selector. J Chromatogr Sci 53(3):431–435
Nie Y, Liu X, Yang X, Zhao Z (2013) Review: Recent application of chiral liquid chromatographytandem mass spectrometric methods for enantiomeric pharmaceutical and biomedical determinations. J Chromatogr Sci 51(8):753–763
Nillos MG, Gan J, Schlenk D (2010) Chirality of organophosphorus pesticides: analysis and
toxicity. J Chromatogr B Analyt Technol Biomed Life Sci 878(17-18):1277–1284
Nishi H, Nagamatsu K (2014) New trend in the LC separation analysis of pharmaceuticals—high
performance separation by ultra high-performance liquid chromatography (UHPLC) with coreshell particle C18 columns. Anal Sci 30(2):205–211
Noctor TA, Wainer IW, Hage DS (1992) Allosteric and competitive displacement of drugs from
human serum albumin by octanoic acid, as revealed by high-performance liquid affinity
chromatography, on a human serum albumin-based stationary phase. J Chromatogr 577
(2):305–315
Novakova L, Vlckova H (2009) A review of current trends and advances in modern bio-analytical
methods: chromatography and sample preparation. Anal Chim Acta 656(1–2):8–35
Novotny MV (2017) Development of capillary liquid chromatography: A personal perspective. J
Chromatogr A 1523:3–16
Nunez O, Gallart-Ayala H, Martins CP, Lucci P (2012) New trends in fast liquid chromatography
for food and environmental analysis. J Chromatogr A 1228:298–323
Okamoto Y, Ikai T (2008) Chiral HPLC for efficient resolution of enantiomers. Chem Soc Rev 37
(12):2593–2608
Okamoto Y, Kawashima M, Aburatani R, Hatada K, Nishiyama T, Masuda M (1986) Optical
resolution of beta-blockers by HPLC on cellulose triphenylcarbamate derivatives. Chem
Lett:1237–1243
O’Mahony J, Clarke L, Whelan M, O’Kennedy R, Lehotay SJ, Danaher M (2013) The use of ultrahigh pressure liquid chromatography with tandem mass spectrometric detection in the analysis
of agrochemical residues and mycotoxins in food - challenges and applications. J Chromatogr A
1292:83–95
Pan C, Wang W, Chen X (2016) [Recent developments of chiral separation by capillary electrophoresis]. Se Pu 34(1):16–20
Patel DC, Wahab MF, Armstrong DW, Breitbach ZS (2016) Advances in high-throughput and
high-efficiency chiral liquid chromatographic separations. J Chromatogr A 1467:2–18
Peluso P, Cossu S, Moretto F, Marchetti M (2009) High performance liquid chromatographic
enantioseparation of chiral bridged polycyclic compounds on chiralcel OD-H and chiralpak OT
(+). Chirality 21(5):507–518
Peluso P, Mamane V, Cossu S (2015) Liquid chromatography enantioseparations of halogenated
compounds on polysaccharide-based chiral stationary phases: role of halogen substituents in
molecular recognition. Chirality 27(10):667–684
Peluso P, Mamane V, Aubert E, Cossu S (2017) Recent trends and applications in liquid-phase
chromatography enantioseparation of atropisomers. Electrophoresis 38(15):1830–1850
Perez-Fernandez V, Garcia MA, Marina ML (2010) Characteristics and enantiomeric analysis of
chiral pyrethroids. J Chromatogr A 1217(7):968–989
Perez-Fernandez V, Garcia MA, Marina ML (2011) Chiral separation of agricultural fungicides. J
Chromatogr A 1218(38):6561–6582
Perisic-Janjic N, Kaliszan R, Wiczling P, Milosevic N, Uscumlic G, Banjac N (2011) Reversedphase TLC and HPLC retention data in correlation studies with in silico molecular descriptors
and druglikeness properties of newly synthesized anticonvulsant succinimide derivatives. Mol
Pharm 8(2):555–563
References
57
recognition: reciprocal chiral-specific DNA binding of synthetic enantiomers of zinc finger
domain from GAGA factor. Chirality 18(4):254–258
Nemeth T, Levai S, Fodi T, Kupai J, Turos G, Toth T, Huszthy P, Balogh GT (2015) A novel
method for the preparation of a chiral stationary phase containing an enantiopure acridino-18crown-6 ether selector. J Chromatogr Sci 53(3):431–435
Nie Y, Liu X, Yang X, Zhao Z (2013) Review: Recent application of chiral liquid chromatographytandem mass spectrometric methods for enantiomeric pharmaceutical and biomedical determinations. J Chromatogr Sci 51(8):753–763
Nillos MG, Gan J, Schlenk D (2010) Chirality of organophosphorus pesticides: analysis and
toxicity. J Chromatogr B Analyt Technol Biomed Life Sci 878(17-18):1277–1284
Nishi H, Nagamatsu K (2014) New trend in the LC separation analysis of pharmaceuticals—high
performance separation by ultra high-performance liquid chromatography (UHPLC) with coreshell particle C18 columns. Anal Sci 30(2):205–211
Noctor TA, Wainer IW, Hage DS (1992) Allosteric and competitive displacement of drugs from
human serum albumin by octanoic acid, as revealed by high-performance liquid affinity
chromatography, on a human serum albumin-based stationary phase. J Chromatogr 577
(2):305–315
Novakova L, Vlckova H (2009) A review of current trends and advances in modern bio-analytical
methods: chromatography and sample preparation. Anal Chim Acta 656(1–2):8–35
Novotny MV (2017) Development of capillary liquid chromatography: A personal perspective. J
Chromatogr A 1523:3–16
Nunez O, Gallart-Ayala H, Martins CP, Lucci P (2012) New trends in fast liquid chromatography
for food and environmental analysis. J Chromatogr A 1228:298–323
Okamoto Y, Ikai T (2008) Chiral HPLC for efficient resolution of enantiomers. Chem Soc Rev 37
(12):2593–2608
Okamoto Y, Kawashima M, Aburatani R, Hatada K, Nishiyama T, Masuda M (1986) Optical
resolution of beta-blockers by HPLC on cellulose triphenylcarbamate derivatives. Chem
Lett:1237–1243
O’Mahony J, Clarke L, Whelan M, O’Kennedy R, Lehotay SJ, Danaher M (2013) The use of ultrahigh pressure liquid chromatography with tandem mass spectrometric detection in the analysis
of agrochemical residues and mycotoxins in food - challenges and applications. J Chromatogr A
1292:83–95
Pan C, Wang W, Chen X (2016) [Recent developments of chiral separation by capillary electrophoresis]. Se Pu 34(1):16–20
Patel DC, Wahab MF, Armstrong DW, Breitbach ZS (2016) Advances in high-throughput and
high-efficiency chiral liquid chromatographic separations. J Chromatogr A 1467:2–18
Peluso P, Cossu S, Moretto F, Marchetti M (2009) High performance liquid chromatographic
enantioseparation of chiral bridged polycyclic compounds on chiralcel OD-H and chiralpak OT
(+). Chirality 21(5):507–518
Peluso P, Mamane V, Cossu S (2015) Liquid chromatography enantioseparations of halogenated
compounds on polysaccharide-based chiral stationary phases: role of halogen substituents in
molecular recognition. Chirality 27(10):667–684
Peluso P, Mamane V, Aubert E, Cossu S (2017) Recent trends and applications in liquid-phase
chromatography enantioseparation of atropisomers. Electrophoresis 38(15):1830–1850
Perez-Fernandez V, Garcia MA, Marina ML (2010) Characteristics and enantiomeric analysis of
chiral pyrethroids. J Chromatogr A 1217(7):968–989
Perez-Fernandez V, Garcia MA, Marina ML (2011) Chiral separation of agricultural fungicides. J
Chromatogr A 1218(38):6561–6582
Perisic-Janjic N, Kaliszan R, Wiczling P, Milosevic N, Uscumlic G, Banjac N (2011) Reversedphase TLC and HPLC retention data in correlation studies with in silico molecular descriptors
and druglikeness properties of newly synthesized anticonvulsant succinimide derivatives. Mol
Pharm 8(2):555–563
References
57