Chiral high-performance liquid and supercritical fluid chromatographic enantioseparations of limonene-based bicyclic aminoalcohols and aminodiols on polysaccharide chiral stationary phases

Chirality is extremely important for the modern pharmaceutical industry since many drug compounds are chiral molecules whose stereoisomers usually possess various toxicological and pharmacological properties. One of the enantiomers (eutomer) have the desired pharmacological activity, while the other...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Orosz Tímea
Németi Gábor
Bajtai Attila
Szakonyi Zsolt
Fülöp Ferenc
Ilisz István
Péter Antal
Testületi szerző: International Symposium on Analytical and Environmental Problems (24.) (2018) (Szeged)
Dokumentumtípus: Könyv része
Megjelent: 2018
Sorozat:Proceedings of the International Symposium on Analytical and Environmental Problems 24
Kulcsszavak:Gyógyszerkémia - előadáskivonat, Analitikai kémia - előadáskivonat
Online Access:http://acta.bibl.u-szeged.hu/56386
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245 1 0 |a Chiral high-performance liquid and supercritical fluid chromatographic enantioseparations of limonene-based bicyclic aminoalcohols and aminodiols on polysaccharide chiral stationary phases  |h [elektronikus dokumentum] /  |c  Orosz Tímea 
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490 0 |a Proceedings of the International Symposium on Analytical and Environmental Problems  |v 24 
520 3 |a Chirality is extremely important for the modern pharmaceutical industry since many drug compounds are chiral molecules whose stereoisomers usually possess various toxicological and pharmacological properties. One of the enantiomers (eutomer) have the desired pharmacological activity, while the other isomer (distomer) is inactive or in worst cases some undesirable effects or even toxic effect can also be produced. The investigated compounds were limonene-based bicyclic 1,3-aminoalcohols and 1,3,5- and 1,3,6-aminodiols. In recent years, these compounds have been intensively investigated due to their potential biological activity and their benefits in synthetic chemistry. Aminoalcohols and aminodiols are known to be outstanding building blocks for the synthesis of remarkable heterocyclic compounds. Aminodiol-based nucleoside analogs possess noteworthy antitumor or antiviral activity [1]. The synthesis of new, limonene-based chiral bicyclic 1,3- aminoalcohols and aminodiols from commercially available starting materials have recently been reported [2]. As a result of the pharmaceutical and biological activity of chiral 1,3-aminoalcohols and aminodiols, it is very important to have at hand enantioselective analytical methods for the identification and separation of these compounds. Enantioseparations of limonene-based bicyclic 1,3-aminoalcohols and 1,3,5- and 1,3,6-aminodiols were carried out with highperformance liquid chromatographic and supercritical fluid chromatographic (SFC) methods on commercial polysaccharide-based chiral stationary phases. The effects of the mobile phase composition, the nature and concentration of the alcohol additive, the temperature and the structures of the studied analytes on the separations were investigated in the normal phase and SFC mode. The elution sequence was determined in all cases. The separations of the stereoisomers of the investigated analytes were optimized in both chromatographic modes. 
695 |a Gyógyszerkémia - előadáskivonat, Analitikai kémia - előadáskivonat 
700 0 1 |a Németi Gábor  |e aut 
700 0 1 |a Bajtai Attila  |e aut 
700 0 1 |a Szakonyi Zsolt  |e aut 
700 0 1 |a Fülöp Ferenc  |e aut 
700 0 1 |a Ilisz István  |e aut 
700 0 1 |a Péter Antal  |e aut 
710 |a International Symposium on Analytical and Environmental Problems (24.) (2018) (Szeged) 
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