134 related articles for article (PubMed ID: 30633381)
1. HPLC with cellulose Tris (3,5-DimethylPhenylcarbamate) chiral stationary phase: Influence of coating times and coating amount on chiral discrimination.
Wei Q; Su H; Gao D; Wang S
Chirality; 2019 Mar; 31(3):164-173. PubMed ID: 30633381
[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. Synthesis and Enantioseparation Ability of Xylan Bisphenylcarbamate Derivatives as Chiral Stationary Phases in HPLC.
Li G; Shen J; Li Q; Okamoto Y
Chirality; 2015 Aug; 27(8):518-22. PubMed ID: 26039871
[TBL] [Abstract][Full Text] [Related]
4. Synthesis of substituted phenylcarbamates of N-cyclobutylformylated chitosan and their application as chiral selectors in enantioseparation.
Zhang J; Wang XC; Chen W; Bai ZW
Analyst; 2016 Jul; 141(14):4470-80. PubMed ID: 27191623
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Controlled synthesis, immobilization and chiral recognition of carboxylic acid functionalized cellulose tris(3,5-dimethylphenylcarbamate).
Han M; Jin X; Yang H; Liu X; Liu Y; Ji S
Carbohydr Polym; 2017 Sep; 172():223-229. PubMed ID: 28606529
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Synthesis of cellulose carbamates bearing regioselective substituents at 2,3- and 6-positions for efficient chromatographic enantioseparation.
Shen J; Wang F; Bi W; Liu B; Liu S; Okamoto Y
J Chromatogr A; 2018 Oct; 1572():54-61. PubMed ID: 30146373
[TBL] [Abstract][Full Text] [Related]
9. Engineering thiol-ene click chemistry for the preparation of a chiral stationary phase based on a [4+6]-type homochiral porous organic cage for enantiomeric separation in normal-phase and reversed-phase high performance liquid chromatography.
Liang RX; Zhang YP; Zhang JH; Gong YN; Huang B; Wang BJ; Xie SM; Yuan LM
J Chromatogr A; 2023 Nov; 1711():464444. PubMed ID: 37837712
[TBL] [Abstract][Full Text] [Related]
10. Green synthesis of a typical chiral stationary phase of cellulose-tris(3, 5-dimethylphenylcarbamate).
Liu RQ; Bai LY; Zhang YJ; Zhang YP
Chem Cent J; 2013 Jul; 7(1):129. PubMed ID: 23890199
[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. [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]
13. 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]
14. Preparation of chiral stationary phase for HPLC based on immobilization of cellulose 3,5-dimethylphenylcarbamate derivatives on silica gel.
Kubota T; Yamamoto C; Okamoto Y
Chirality; 2003 Jan; 15(1):77-82. PubMed ID: 12467047
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Preparation and Enantioseparation of Biselector Chiral Stationary Phases Based on Amylose and Chitin Derivatives.
Zhang J; Wang ZQ; Chen W; Bai ZW
Anal Sci; 2015; 31(10):1091-7. PubMed ID: 26460376
[TBL] [Abstract][Full Text] [Related]
17. Preparation and evaluation of regioselectively substituted amylose derivatives for chiral separations.
Tang S; Jin Z; Sun B; Wang F; Tang W
Chirality; 2017 Sep; 29(9):512-521. PubMed ID: 28635058
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Synthesis and HPLC chiral recognition of regioselectively carbamoylated cellulose derivatives.
Tang S; Li X; Wang F; Liu G; Li Y; Pan F
Chirality; 2012 Feb; 24(2):167-73. PubMed ID: 22213581
[TBL] [Abstract][Full Text] [Related]
20. Synthesis and characterization of cellulose 3,5-dimethylphenylcarbamate silica hybrid spheres for enantioseparation of chiral β-blockers.
Weng X; Bao Z; Xing H; Zhang Z; Yang Q; Su B; Yang Y; Ren Q
J Chromatogr A; 2013 Dec; 1321():38-47. PubMed ID: 24231262
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]