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Results: 1-8 |
Results: 8
Mechanism of chiral recognition in the enantioseparation of 2-aryloxypropionic acids on new brush-type chiral stationary phases
Authors: Vinkovic, V Kontrec, D Sunjic, V Navarini, L Zanetti, F Azzolina, O
Citation: V. Vinkovic et al., Mechanism of chiral recognition in the enantioseparation of 2-aryloxypropionic acids on new brush-type chiral stationary phases, CHIRALITY, 13(9), 2001, pp. 581-587
Solid-phase synthesis of chiral stationary phases based on 2,4,5,6-tetrachloro-1,3-dicyanobenzene derivatives spaced from N-3,5-dinitrobenzoyl alpha-amino acids: Comparative study of their resolution efficacy
Authors: Kontrec, D Abatangelo, A Vinkovic, V Sunjic, V
Citation: D. Kontrec et al., Solid-phase synthesis of chiral stationary phases based on 2,4,5,6-tetrachloro-1,3-dicyanobenzene derivatives spaced from N-3,5-dinitrobenzoyl alpha-amino acids: Comparative study of their resolution efficacy, CHIRALITY, 13(6), 2001, pp. 294-301
Preparation and evaluation of the chiral stationary phases based on N-4-(2,5,6-trichloro-1,3-dicyano)-phenyl derivatives of L-alpha-amino acids
Authors: Kontrec, D Vinkovic, V Sunjic, V
Citation: D. Kontrec et al., Preparation and evaluation of the chiral stationary phases based on N-4-(2,5,6-trichloro-1,3-dicyano)-phenyl derivatives of L-alpha-amino acids, J LIQ CHR R, 23(8), 2000, pp. 1203-1215
Novel chiral stationary phases comprising 2,4-(or 2,6)-diamino-5,6-(or 2,5)-dichlorobenzene-1,3-dicarbonitrile and 1-acyl (1R,2R)-diaminocyclohexane
Authors: Kontrec, D Vinkovic, V Lesac, A Sunjia, V Aced, A
Citation: D. Kontrec et al., Novel chiral stationary phases comprising 2,4-(or 2,6)-diamino-5,6-(or 2,5)-dichlorobenzene-1,3-dicarbonitrile and 1-acyl (1R,2R)-diaminocyclohexane, ENANTIOMER, 5(3-4), 2000, pp. 333-344
Preparation and evaluation of chiral stationary phases based on N,N-2,4-(or 4,8)-disubstituted 4,5-(or 2,5)-dichloro-1,3-dicyanobenzene
Authors: Kontrec, D Vinkovic, V Sunjic, V
Citation: D. Kontrec et al., Preparation and evaluation of chiral stationary phases based on N,N-2,4-(or 4,8)-disubstituted 4,5-(or 2,5)-dichloro-1,3-dicyanobenzene, CHIRALITY, 12(2), 2000, pp. 63-70
Electronic structure of persubstituted benzenes: caveats
Authors: Novak, I Kovac, B Kontrec, D Sunjic, V
Citation: I. Novak et al., Electronic structure of persubstituted benzenes: caveats, J ELEC SPEC, 109(3), 2000, pp. 281-286
Chiroptical and conformational properties of (R)-1-phenylethylamine derivatives of persubstituted benzene
Authors: Kontrec, D Vinkovic, V Lesac, A Sunjic, V Hollosi, M
Citation: D. Kontrec et al., Chiroptical and conformational properties of (R)-1-phenylethylamine derivatives of persubstituted benzene, TETRAHEDR-A, 10(10), 1999, pp. 1935-1945
New chiral stationary phases based on (R)-1-naphthylethylamine bound to 2,4,5,6-tetrachloro-1,3-dicyanobenzene
Authors: Kontrec, D Vinkovic, V Sunjic, V
Citation: D. Kontrec et al., New chiral stationary phases based on (R)-1-naphthylethylamine bound to 2,4,5,6-tetrachloro-1,3-dicyanobenzene, CHIRALITY, 11(9), 1999, pp. 722-730
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