Understanding the Transition from High-Selective to High-Efficient Chiral Separations by Changing the Organic Modifier with Zwitterionic-Teicoplanin Chiral Stationary Phase-Reference-Cited by-同舟云学术

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Understanding the Transition from High-Selective to High-Efficient Chiral Separations by Changing the Organic Modifier with Zwitterionic-Teicoplanin Chiral Stationary Phase

Published:2023-06-09 Issue:25 Volume:95 Page:9630-9637
ISSN:0003-2700
Container-title:Analytical Chemistry
language:en
Short-container-title:Anal. Chem.

Author:

Felletti Simona¹^ORCID,De Luca Chiara¹^ORCID,Mazzoccanti Giulia²^ORCID,Gasparrini Francesco²^ORCID,Manetto Simone²,Franchina Flavio Antonio¹,Chenet Tatiana³,Pasti Luisa³^ORCID,Cavazzini Alberto¹,Catani Martina¹^ORCID

Affiliation:

1. Department of Chemical, Pharmaceutical and Agricultural Sciences, University of Ferrara, via L. Borsari 46, 44121 Ferrara, Italy

2. Department of Drug Chemistry and Technology, “Sapienza” University of Rome, P. le Aldo Moro 5, 00185 Rome, Italy

3. Department of Environmental and Prevention Sciences, University of Ferrara, via L. Borsari 46, 44121 Ferrara, Italy

Funder

European Commission

Ministero dell'Universit? e della Ricerca

Publisher

American Chemical Society (ACS)

Subject

Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.analchem.3c01344

Reference41 articles.

1. Future perspectives in high efficient and ultrafast chiral liquid chromatography through zwitterionic teicoplanin-based 2-μm superficially porous particles

2. Direct analysis of chiral active pharmaceutical ingredients and their counterions by ultra high performance liquid chromatography with macrocyclic glycopeptide-based chiral stationary phases

3. Study of mechanisms of chiral discrimination of amino acids and their derivatives on a teicoplanin-based chiral stationary phase

4. Boosting the enantioresolution of zwitterionic-teicoplanin chiral stationary phases by moving to wide-pore core-shell particles

5. High–throughput enantioseparation of Nα–fluorenylmethoxycarbonyl proteinogenic amino acids through fast chiral chromatography on zwitterionic-teicoplanin stationary phases

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1. Synergetic Multichiral Covalent Organic Framework for Enantioselective Recognition and Separation;Analytical Chemistry;2024-01-10

2. Recent developments in the high-throughput separation of biologically active chiral compounds via high performance liquid chromatography;Journal of Pharmaceutical and Biomedical Analysis;2024-01

3. Dimethyl carbonate as a green alternative to acetonitrile in reversed-phase liquid chromatography. Part I: Separation of small molecules;Journal of Chromatography A;2023-12

4. Automated sample preparation with 6-Aminoquinolyl-N-hydroxysuccinimidyl carbamate and iodoacetamide derivatization reagents for enantioselective liquid chromatography tandem mass spectrometry amino acid analysis;Journal of Chromatography A;2023-10

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