225 related articles for article (PubMed ID: 32505273)
1. Chiral stationary phase based on cellulose derivative coated polymer microspheres and its separation performance.
Li L; Yuan XT; Shi ZG; Xu LY
J Chromatogr A; 2020 Jul; 1623():461154. PubMed ID: 32505273
[TBL] [Abstract][Full Text] [Related]
2. Chiral stationary phases based on chitosan bis(methylphenylcarbamate)-(isobutyrylamide) for high-performance liquid chromatography.
Tang S; Bin Q; Chen W; Bai ZW; Huang SH
J Chromatogr A; 2016 Apr; 1440():112-122. PubMed ID: 26931425
[TBL] [Abstract][Full Text] [Related]
3. Fabrication of cellulose derivative coated spherical covalent organic frameworks as chiral stationary phases for high-performance liquid chromatographic enantioseparation.
Yan YL; Guo D; Wu JL; Tang XH; Luo JJ; Li SQ; Fan J; Zheng SR; Zhang WG; Cai SL
J Chromatogr A; 2022 Jul; 1675():463155. PubMed ID: 35635867
[TBL] [Abstract][Full Text] [Related]
4. Enantioseparation characteristics of biselector chiral stationary phases based on derivatives of cellulose and amylose.
Wang ZQ; Liu JD; Chen W; Bai ZW
J Chromatogr A; 2014 Jun; 1346():57-68. PubMed ID: 24792697
[TBL] [Abstract][Full Text] [Related]
5. Comparative high-performance liquid chromatography enantioseparations on polysaccharide based chiral stationary phases prepared by coating totally porous and core-shell silica particles.
Lomsadze K; Jibuti G; Farkas T; Chankvetadze B
J Chromatogr A; 2012 Apr; 1234():50-5. PubMed ID: 22349144
[TBL] [Abstract][Full Text] [Related]
6. Reversed-phase chiral HPLC and LC/MS analysis with tris(chloromethylphenylcarbamate) derivatives of cellulose and amylose as chiral stationary phases.
Peng L; Jayapalan S; Chankvetadze B; Farkas T
J Chromatogr A; 2010 Oct; 1217(44):6942-55. PubMed ID: 20863505
[TBL] [Abstract][Full Text] [Related]
7. [Preparation and evaluation of amylose and cellulose tris (3-trifluoromethylphenylcarbamates)-based chiral stationary phases].
Jin Z; Hu F; Wang Y; Liu G; Wang F; Pan F; Tang S
Se Pu; 2011 Nov; 29(11):1087-92. PubMed ID: 22393696
[TBL] [Abstract][Full Text] [Related]
8. Nanocellulose 3, 5-Dimethylphenylcarbamate Derivative Coated Chiral Stationary Phase: Preparation and Enantioseparation Performance.
Zhang X; Wang L; Dong S; Zhang X; Wu Q; Zhao L; Shi Y
Chirality; 2016 May; 28(5):376-81. PubMed ID: 26949227
[TBL] [Abstract][Full Text] [Related]
9. Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition.
Shibata T; Shinkura S; Ohnishi A; Ueda K
Molecules; 2016 Dec; 22(1):. PubMed ID: 28036038
[TBL] [Abstract][Full Text] [Related]
10. Cellulose tris(3,5-dimethylphenylcarbamate)-coated zirconia as a chiral stationary phase for HPLC.
Castells CB; Carr PW
Anal Chem; 1999 Aug; 71(15):3013-21. PubMed ID: 10450151
[TBL] [Abstract][Full Text] [Related]
11. High-performance liquid chromatographic evaluation of a coated cellulose tris(3,5-dimethylphenylcarbamate) chiral stationary phase having a small-pore silica support.
Liu Y; Zou H
J Chromatogr A; 2008 Jan; 1178(1-2):118-25. PubMed ID: 18068714
[TBL] [Abstract][Full Text] [Related]
12. Flow-through silica: A potential matrix for fast chromatographic enantioseparation with high enantioselectivity.
Mao XJ; Li J; Liu D; Qiao T; Ma L; Sun X; Xu L; Shi ZG
Talanta; 2018 Feb; 178():583-587. PubMed ID: 29136866
[TBL] [Abstract][Full Text] [Related]
13. Enantioseparation Using Cellulose Tris(3,5-dimethylphenylcarbamate) as Chiral Stationary Phase for HPLC: Influence of Molecular Weight of Cellulose.
Okada Y; Yamamoto C; Kamigaito M; Gao Y; Shen J; Okamoto Y
Molecules; 2016 Nov; 21(11):. PubMed ID: 27834832
[TBL] [Abstract][Full Text] [Related]
14. Enantioseparation and molecular modeling study of chiral amines as three naphthaldimine derivatives using amylose or cellulose trisphenylcarbamate chiral stationary phases.
Adhikari S; Bhujbal S; Paik MJ; Lee W
Chirality; 2023 Jan; 35(1):29-39. PubMed ID: 36323631
[TBL] [Abstract][Full Text] [Related]
15. Monolithic silica capillary columns with immobilized cellulose tris(3,5-dimethylphenylcarbamate) for enantiomer separations in CEC.
He C; Hendrickx A; Mangelings D; Smeyers-Verbeke J; Vander Heyden Y
Electrophoresis; 2009 Nov; 30(22):3796-803. PubMed ID: 19885889
[TBL] [Abstract][Full Text] [Related]
16. Cellulose tris(3,5-dichlorophenylcarbamate) immobilised on silica: a novel chiral stationary phase for resolution of enantiomers.
Zhang T; Nguyen D; Franco P; Isobe Y; Michishita T; Murakami T
J Pharm Biomed Anal; 2008 Apr; 46(5):882-91. PubMed ID: 17658716
[TBL] [Abstract][Full Text] [Related]
17. Application of cellulose 3,5-dichlorophenylcarbamate covalently immobilized on superficially porous silica for the separation of enantiomers in high-performance liquid chromatography.
Bezhitashvili L; Bardavelidze A; Mskhiladze A; Gumustas M; Ozkan SA; Volonterio A; Farkas T; Chankvetadze B
J Chromatogr A; 2018 Oct; 1571():132-139. PubMed ID: 30098733
[TBL] [Abstract][Full Text] [Related]
18. Synthesis and enantioseparation behaviors of novel immobilized 3,5-dimethylphenylcarbamoylated polysaccharide chiral stationary phases.
Tan Y; Fan J; Lin C; Tu H; Zheng S; Zhang W
J Sep Sci; 2014 Mar; 37(5):488-94. PubMed ID: 24376089
[TBL] [Abstract][Full Text] [Related]
19. Enantioseparations with cellulose tris(3-chloro-4-methylphenylcarbamate) in nano-liquid chromatography and capillary electrochromatography.
Fanali S; D'Orazio G; Lomsadze K; Chankvetadze B
J Chromatogr B Analyt Technol Biomed Life Sci; 2008 Nov; 875(1):296-303. PubMed ID: 18691950
[TBL] [Abstract][Full Text] [Related]
20. Preparation and characterization of monodisperse large-porous silica microspheres as the matrix for protein separation.
Xia H; Wan G; Zhao J; Liu J; Bai Q
J Chromatogr A; 2016 Nov; 1471():138-144. PubMed ID: 27765422
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
