126 related articles for article (PubMed ID: 28606529)
1. 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]
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. Improved preparation of chiral stationary phases via immobilization of polysaccharide derivative-based selectors using diisocyanates.
Tang S; Liu G; Li X; Jin Z; Wang F; Pan F; Okamoto Y
J Sep Sci; 2011 Aug; 34(15):1763-71. PubMed ID: 21688393
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Photochemically Immobilized 4-Methylbenzoyl Cellulose as a Powerful Chiral Stationary Phase for Enantioselective Chromatography.
Francotte E; Huynh D; Zhang T
Molecules; 2016 Dec; 21(12):. PubMed ID: 27999329
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Synthesis and application of immobilized polysaccharide-based chiral stationary phases for enantioseparation by high-performance liquid chromatography.
Shen J; Ikai T; Okamoto Y
J Chromatogr A; 2014 Oct; 1363():51-61. PubMed ID: 24997110
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Synthesis of chiral stationary phases with radical polymerization reaction of cellulose phenylcarbamate derivatives and vinylized silica gel.
Chen X; Qin F; Liu Y; Huang X; Zou H
J Chromatogr A; 2004 Apr; 1034(1-2):109-16. PubMed ID: 15116919
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Characteristic and complementary chiral recognition ability of four recently developed immobilized chiral stationary phases based on amylose and cellulose phenyl carbamates and benzoates.
Onishi T; Ueda T; Yoshida K; Uosaki K; Ando H; Hamasaki R; Ohnishi A
Chirality; 2022 Jul; 34(7):925-940. PubMed ID: 35413148
[TBL] [Abstract][Full Text] [Related]
15. Influence of vinyl monomers and temperature on immobilization of cellulose 3,5-dimethylphenylcarbamate onto silica gel as chiral stationary phases for high-performance liquid chromatography.
Chen XM; Yamamoto C; Okamoto Y
J Chromatogr A; 2006 Feb; 1104(1-2):62-8. PubMed ID: 16359692
[TBL] [Abstract][Full Text] [Related]
16. High performance chiral separation materials based on chitosan bis(3,5-dimethylphenylcarbamate)-(alkyl urea)s.
Wang J; Xi JB; Chen W; Huang SH; Bai ZW
Carbohydr Polym; 2017 Jan; 156():481-489. PubMed ID: 27842849
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]