Ghosn MW, Wolf C (2011) Synthesis, conformational stability, and asymmetric transformation of
atropisomeric 1,8-bisphenolnaphthalenes. J Org Chem 76(10):3888–3897
Glunz PW (2018) Recent encounters with atropisomerism in drug discovery. Bioorg Med Chem
Lett 28(2):53–60
Golubovic J, Protic A, Otasevic B, Zecevic M (2016) Quantitative structure-retention relationships
applied to development of liquid chromatography gradient-elution method for the separation of
sartans. Talanta 150:190–197
Guo Y, Gaiki S (2011) Retention and selectivity of stationary phases for hydrophilic interaction
chromatography. J Chromatogr A 1218(35):5920–5938
Guo F, Zhang J, Wang C (2017) Enantioselectivity in environmental safety and metabolism of
typical chiral organic pollutants. Curr Protein Pept Sci 18(1):4–9
Hayward SJ, Lei YD, Wania F (2006) Comparative evaluation of three high-performance liquid
chromatography-based Kow estimation methods for highly hydrophobic organic compounds:
polybrominated diphenyl ethers and hexabromocyclododecane. Environ Toxicol Chem 25
(8):2018–2027
Hesek D, Hembury GA, Drew MG, Borovkov VV, Inoue Y (2001) Photochromic atropisomer
generation and conformation determination in a ruthenium bis(bipyridine) phosphonite gammacyclodextrin system. J Am Chem Soc 123(49):12232–12237
Hu YL, Ziffer H (1991) A new model to account for the order in which enantiomers of
alkylarylcarbinols elute from a Pirkle chiral HPLC column: preparation, absolute stereochemistry, and chromatographic properties of (+)-1,2-benzocyclononen-3-ol and (+)-1,2benzocyclodecen-3-ol. Chirality 3(3):196–203
Hühnerfuss H, Shah MR (2009) Enantioselective chromatography-a powerful tool for the discrimination of biotic and abiotic transformation processes of chiral environmental pollutants. J
Chromatogr A 1216(3):481–502
Inoue Y, Ramamurthy V (2004) Chiral photochemistry. Marcel Dekker, New York
Jandera P, Hajek T (2018) Mobile phase effects on the retention on polar columns with special
attention to the dual hydrophilic interaction-reversed-phase liquid chromatography mechanism,
a review. J Sep Sci 41(1):145–162
Jandera P, Janas P (2017) Recent advances in stationary phases and understanding of retention in
hydrophilic interaction chromatography. A review. Anal Chim Acta 967:12–32
Jian W, Xu Y, Edom RW, Weng N (2011) Analysis of polar metabolites by hydrophilic interaction
chromatography--MS/MS. Bioanalysis 3(8):899–912
Jurcek O, Bonakdarzadeh P, Kalenius E, Linnanto JM, Groessl M, Knochenmuss R, Ihalainen JA,
Rissanen K (2015) Superchiral Pd3 L6 coordination complex and its reversible structural
conversion into Pd3 L3 Cl6 Metallocycles. Angew Chem Int Ed Engl 54(51):15462–15467
Kah M, Brown CD (2008) LogD: lipophilicity for ionisable compounds. Chemosphere 72
(10):1401–1408
Kalachova K, Pulkrabova J, Cajka T, Drabova L, Stupak M, Hajslova J (2013) Gas
chromatography-triple quadrupole tandem mass spectrometry: a powerful tool for the (ultra)trace analysis of multiclass environmental contaminants in fish and fish feed. Anal Bioanal
Chem 405(24):7803–7815
Kania-Korwel I, Lehmler HJ (2016) Toxicokinetics of chiral polychlorinated biphenyls across
different species--a review. Environ Sci Pollut Res Int 23(3):2058–2080
Kasprzyk-Hordern B (2010) Pharmacologically active compounds in the environment and their
chirality. Chem Soc Rev 39(11):4466–4503
Kazsoki A, Fejos I, Sohajda T, Zhou W, Hu W, Szente L, Beni S (2016) Development and
validation of a cyclodextrin-modified capillary electrophoresis method for the enantiomeric
separation of vildagliptin enantiomers. Electrophoresis 37(10):1318–1325
Kim SJ, Lee H, Kwon JH (2014) Measurement of partition coefficients for selected polycyclic
aromatic hydrocarbons between isolated plant cuticles and water. Sci Total Environ
494-495:113–118
References
25
atropisomeric 1,8-bisphenolnaphthalenes. J Org Chem 76(10):3888–3897
Glunz PW (2018) Recent encounters with atropisomerism in drug discovery. Bioorg Med Chem
Lett 28(2):53–60
Golubovic J, Protic A, Otasevic B, Zecevic M (2016) Quantitative structure-retention relationships
applied to development of liquid chromatography gradient-elution method for the separation of
sartans. Talanta 150:190–197
Guo Y, Gaiki S (2011) Retention and selectivity of stationary phases for hydrophilic interaction
chromatography. J Chromatogr A 1218(35):5920–5938
Guo F, Zhang J, Wang C (2017) Enantioselectivity in environmental safety and metabolism of
typical chiral organic pollutants. Curr Protein Pept Sci 18(1):4–9
Hayward SJ, Lei YD, Wania F (2006) Comparative evaluation of three high-performance liquid
chromatography-based Kow estimation methods for highly hydrophobic organic compounds:
polybrominated diphenyl ethers and hexabromocyclododecane. Environ Toxicol Chem 25
(8):2018–2027
Hesek D, Hembury GA, Drew MG, Borovkov VV, Inoue Y (2001) Photochromic atropisomer
generation and conformation determination in a ruthenium bis(bipyridine) phosphonite gammacyclodextrin system. J Am Chem Soc 123(49):12232–12237
Hu YL, Ziffer H (1991) A new model to account for the order in which enantiomers of
alkylarylcarbinols elute from a Pirkle chiral HPLC column: preparation, absolute stereochemistry, and chromatographic properties of (+)-1,2-benzocyclononen-3-ol and (+)-1,2benzocyclodecen-3-ol. Chirality 3(3):196–203
Hühnerfuss H, Shah MR (2009) Enantioselective chromatography-a powerful tool for the discrimination of biotic and abiotic transformation processes of chiral environmental pollutants. J
Chromatogr A 1216(3):481–502
Inoue Y, Ramamurthy V (2004) Chiral photochemistry. Marcel Dekker, New York
Jandera P, Hajek T (2018) Mobile phase effects on the retention on polar columns with special
attention to the dual hydrophilic interaction-reversed-phase liquid chromatography mechanism,
a review. J Sep Sci 41(1):145–162
Jandera P, Janas P (2017) Recent advances in stationary phases and understanding of retention in
hydrophilic interaction chromatography. A review. Anal Chim Acta 967:12–32
Jian W, Xu Y, Edom RW, Weng N (2011) Analysis of polar metabolites by hydrophilic interaction
chromatography--MS/MS. Bioanalysis 3(8):899–912
Jurcek O, Bonakdarzadeh P, Kalenius E, Linnanto JM, Groessl M, Knochenmuss R, Ihalainen JA,
Rissanen K (2015) Superchiral Pd3 L6 coordination complex and its reversible structural
conversion into Pd3 L3 Cl6 Metallocycles. Angew Chem Int Ed Engl 54(51):15462–15467
Kah M, Brown CD (2008) LogD: lipophilicity for ionisable compounds. Chemosphere 72
(10):1401–1408
Kalachova K, Pulkrabova J, Cajka T, Drabova L, Stupak M, Hajslova J (2013) Gas
chromatography-triple quadrupole tandem mass spectrometry: a powerful tool for the (ultra)trace analysis of multiclass environmental contaminants in fish and fish feed. Anal Bioanal
Chem 405(24):7803–7815
Kania-Korwel I, Lehmler HJ (2016) Toxicokinetics of chiral polychlorinated biphenyls across
different species--a review. Environ Sci Pollut Res Int 23(3):2058–2080
Kasprzyk-Hordern B (2010) Pharmacologically active compounds in the environment and their
chirality. Chem Soc Rev 39(11):4466–4503
Kazsoki A, Fejos I, Sohajda T, Zhou W, Hu W, Szente L, Beni S (2016) Development and
validation of a cyclodextrin-modified capillary electrophoresis method for the enantiomeric
separation of vildagliptin enantiomers. Electrophoresis 37(10):1318–1325
Kim SJ, Lee H, Kwon JH (2014) Measurement of partition coefficients for selected polycyclic
aromatic hydrocarbons between isolated plant cuticles and water. Sci Total Environ
494-495:113–118
References
25