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
Author:
Funder
Ministry of Human Capacities
Publisher
Elsevier BV
Subject
Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry
Reference32 articles.
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2. Quantitative determination of major alkaloids in Cinchona bark by Supercritical Fluid Chromatography;Murauer;J. Chromatogr. A,2018
3. Separation of Cinchona alkaloids on a novel strong cation-exchange-type chiral stationary phase—comparison with commercially available strong cation exchanger and reversed-phase packing materials;Hoffmann;Anal. Bioanal. Chem.,2009
4. A Local-desymmetrization-based divergent synthesis of quinine and quinidine;Lee;Angew. Chem.,2019
5. C−H Activation enables a concise total synthesis of quinine and analogues with enhanced antimalarial activity;O' Donovan;Angew. Chem. Int. Ed.,2018
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3. Efficient enantioresolution of aromatic α-hydroxy acids with Cinchona alkaloid-based zwitterionic stationary phases and volatile polar-ionic eluents;Analytica Chimica Acta;2021-10
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