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Liquid chromatographic resolution of natural and racemic Cinchona alkaloid analogues using strong cation- and zwitterion ion-exchange type stationary phases. Qualitative evaluation of stationary phase characteristics and mobile phase effects on stereoselectivity and retention.
Bajtai A, Ilisz I, Péter A, Lindner W. Bajtai A, et al. J Chromatogr A. 2020 Jan 4;1609:460498. doi: 10.1016/j.chroma.2019.460498. Epub 2019 Aug 30. J Chromatogr A. 2020. PMID: 31526638
Enantioseparation of ß-carboline, tetrahydroisoquinoline and benzazepine analogues of pharmaceutical importance: Utilization of chiral stationary phases based on polysaccharides and sulfonic acid modified Cinchonaalkaloids in high-performance liquid and subcritical fluid chromatography.
Ilisz I, Bajtai A, Szatmári I, Fülöp F, Lindner W, Péter A. Ilisz I, et al. Among authors: bajtai a. J Chromatogr A. 2020 Mar 29;1615:460771. doi: 10.1016/j.chroma.2019.460771. Epub 2019 Dec 5. J Chromatogr A. 2020. PMID: 31839353 Free article.
High-performance liquid chromatographic evaluation of strong cation exchanger-based chiral stationary phases focusing on stationary phase characteristics and mobile phase effects employing enantiomers of tetrahydro-ß-carboline and 1,2,3,4-tetrahydroisoquinoline analogs.
Bajtai A, Tanács D, Berkecz R, Forró E, Fülöp F, Lindner W, Péter A, Ilisz I. Bajtai A, et al. J Chromatogr A. 2021 May 10;1644:462121. doi: 10.1016/j.chroma.2021.462121. Epub 2021 Mar 31. J Chromatogr A. 2021. PMID: 33845425 Free article.
83 results