Liquid chromatographic enantioseparation of limonene-based carbocyclic β-amino acids on zwitterionic Cinchona alkaloid-based chiral stationary phases

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Liquid chromatographic enantioseparation of limonene-based carbocyclic β-amino acids on zwitterionic Cinchona alkaloid-based chiral stationary phases

The eight stereoisomers of limonene-based carbocyclic β-amino acids containing three chiral centers have been directly separated on chiral stationary phases containing Cinchona alkaloid-based zwitterionic selectors. The effects of bulk solvent composition of the mobile phase, the nature of base addi...

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Bibliográfiai részletek
Szerzők:	Lajkó Gyula Orosz Tímea Ugrai Imre Szakonyi Zsolt Fülöp Ferenc Lindner Wolfgang Péter Antal Ilisz István
Dokumentumtípus:	Cikk
Megjelent:	2017
Sorozat:	JOURNAL OF SEPARATION SCIENCE 40 No. 16
doi:	10.1002/jssc.201700450
mtmt:	3283443
Online Access:	http://publicatio.bibl.u-szeged.hu/12511

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