Lindner W - Search Results

1

Cinchona Alkaloid-Based Zwitterionic Chiral Stationary Phases Applied for Liquid Chromatographic Enantiomer Separations: An Overview.

Ilisz I, Bajtai A, Péter A, Lindner W. Ilisz I, et al. Among authors: lindner w. Methods Mol Biol. 2019;1985:251-277. doi: 10.1007/978-1-4939-9438-0_14. Methods Mol Biol. 2019. PMID: 31069739 Review.

2

Computerized optimization of the high-performance liquid chromatographic enantioseparation of a mixture of 4-dinitrophenyl amino acids on a quinine carbamate-type chiral stationary phase using DRYLAB.

Lämmerhofer M, Di Eugenio P, Molnar I, Lindner W. Lämmerhofer M, et al. Among authors: lindner w. J Chromatogr B Biomed Sci Appl. 1997 Feb 7;689(1):123-35. doi: 10.1016/s0378-4347(96)00366-0. J Chromatogr B Biomed Sci Appl. 1997. PMID: 9061488

3

Enantioselective anion exchangers based on cinchona alkaloid-derived carbamates: influence of C8/C9 stereochemistry on chiral recognition.

Maier NM, Nicoletti L, Lämmerhofer M, Lindner W. Maier NM, et al. Among authors: lindner w. Chirality. 1999;11(7):522-8. doi: 10.1002/(SICI)1520-636X(1999)11:7<522::AID-CHIR2>3.0.CO;2-U. Chirality. 1999. PMID: 10423277

4

Novel cinchona alkaloid carbamate C9-dimers as chiral anion-exchange type selectors for high-performance liquid chromatography.

Franco P, Lämmerhofer M, Klaus PM, Lindner W. Franco P, et al. Among authors: lindner w. J Chromatogr A. 2000 Feb 11;869(1-2):111-27. doi: 10.1016/s0021-9673(99)00877-8. J Chromatogr A. 2000. PMID: 10720230

5

Investigation of an enantioselective non-aqueous capillary electrochromatography system applied to the separation of chiral acids.

Tobler E, Lämmerhofer M, Lindner W. Tobler E, et al. Among authors: lindner w. J Chromatogr A. 2000 Apr 14;875(1-2):341-52. doi: 10.1016/s0021-9673(99)01302-3. J Chromatogr A. 2000. PMID: 10839154

6

Chiral anion exchangers applied to capillary electrochromatography enantioseparation of oppositely charged chiral analytes: investigation of stationary and mobile phase parameters.

Lämmerhofer M, Tobler E, Lindner W. Lämmerhofer M, et al. Among authors: lindner w. J Chromatogr A. 2000 Jul 28;887(1-2):421-37. doi: 10.1016/s0021-9673(99)01329-1. J Chromatogr A. 2000. PMID: 10961331

7

Comparative molecular field analysis of quinine derivatives used as chiral selectors in liquid chromatography: 3D QSAR for the purposes of molecular design of chiral stationary phases.

Schefzick S, Lämmerhofer M, Lindner W, Lipkowitz KB, Jalaie M. Schefzick S, et al. Among authors: lindner w. Chirality. 2000 Nov;12(10):742-50. doi: 10.1002/1520-636X(2000)12:10<742::AID-CHIR7>3.0.CO;2-M. Chirality. 2000. PMID: 11054833

8

Elucidation of the chiral recognition mechanism of cinchona alkaloid carbamate-type receptors for 3,5-dinitrobenzoyl amino acids.

Maier NM, Schefzick S, Lombardo GM, Feliz M, Rissanen K, Lindner W, Lipkowitz KB. Maier NM, et al. Among authors: lindner w. J Am Chem Soc. 2002 Jul 24;124(29):8611-29. doi: 10.1021/ja020203i. J Am Chem Soc. 2002. PMID: 12121103

9

Enantioseparation of various amino acid derivatives on a quinine based chiral anion-exchange selector at variable temperature conditions. Influence of structural parameters of the analytes on the apparent retention and enantioseparation characteristics.

Oberleitner WR, Maier NM, Lindner W. Oberleitner WR, et al. Among authors: lindner w. J Chromatogr A. 2002 Jun 25;960(1-2):97-108. doi: 10.1016/s0021-9673(02)00244-3. J Chromatogr A. 2002. PMID: 12150567

10

Direct high-performance liquid chromatographic separation of peptide enantiomers: study on chiral recognition by systematic evaluation of the influence of structural features of the chiral selectors on enantioselectivity.

Czerwenka C, Lämmerhofer M, Maier NM, Rissanen K, Lindner W. Czerwenka C, et al. Among authors: lindner w. Anal Chem. 2002 Nov 1;74(21):5658-66. doi: 10.1021/ac020372l. Anal Chem. 2002. PMID: 12433102

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