245 related articles for article (PubMed ID: 29174571)
1. A chromatographic study on the exceptional chiral recognition of 2-(benzylsulfinyl)benzamide by an immobilized-type chiral stationary phase based on cellulose tris(3,5-dichlorophenylcarbamate).
Carradori S; Secci D; Faggi C; Cirilli R
J Chromatogr A; 2018 Jan; 1531():151-156. PubMed ID: 29174571
[TBL] [Abstract][Full Text] [Related]
2. High-performance liquid chromatography enantioseparation of chiral 2-(benzylsulfinyl)benzamide derivatives on cellulose tris(3,5-dichlorophenylcarbamate) chiral stationary phase.
Carradori S; Secci D; Guglielmi P; Pierini M; Cirilli R
J Chromatogr A; 2020 Jan; 1610():460572. PubMed ID: 31606155
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Enantioseparation of selected chiral sulfoxides using polysaccharide-type chiral stationary phases and polar organic, polar aqueous-organic and normal-phase eluents.
Chankvetadze B; Yamamoto C; Okamoto Y
J Chromatogr A; 2001 Jul; 922(1-2):127-37. PubMed ID: 11486857
[TBL] [Abstract][Full Text] [Related]
5. Thermodynamic evaluation of immobilized cellulose tris(3,5-dichlorophenylcarbamate) as a stationary phase for liquid chromatographic separation of darunavir enantiomers.
Nageswara Rao R; Nagesh Kumar K
J Chromatogr Sci; 2015 Feb; 53(2):295-301. PubMed ID: 24952101
[TBL] [Abstract][Full Text] [Related]
6. Exploring solvent versatility in immobilized cellulose-based chiral stationary phase for the enantioselective liquid chromatographic resolution of racemates.
Ghanem A
J Sep Sci; 2007 May; 30(7):1019-28. PubMed ID: 17566336
[TBL] [Abstract][Full Text] [Related]
7. Separation of enantiomers of selected chiral sulfoxides with cellulose tris(4-chloro-3-methylphenylcarbamate)-based chiral columns in high-performance liquid chromatography with very high separation factor.
Khatiashvili T; Kakava R; Matarashvili I; Tabani H; Fanali C; Volonterio A; Farkas T; Chankvetadze B
J Chromatogr A; 2018 Apr; 1545():59-66. PubMed ID: 29502898
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Comparative study of coated and immobilized polysaccharide-based chiral stationary phases and their applicability in the resolution of enantiomers.
Thunberg L; Hashemi J; Andersson S
J Chromatogr B Analyt Technol Biomed Life Sci; 2008 Nov; 875(1):72-80. PubMed ID: 18723406
[TBL] [Abstract][Full Text] [Related]
10. Separation of eight bedaquiline analogue diastereomers by HPLC on an immobilized polysaccharide-based chiral stationary phase.
Jiang S; Wu C; Yu J; Sun T; Guo X
Chirality; 2019 Jan; 31(1):72-78. PubMed ID: 30515892
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Separation of enantiomers of chiral sulfoxides in high-performance liquid chromatography with cellulose-based chiral selectors using methanol and methanol-water mixtures as mobile phases.
Shedania Z; Kakava R; Volonterio A; Farkas T; Chankvetadze B
J Chromatogr A; 2018 Jul; 1557():62-74. PubMed ID: 29748092
[TBL] [Abstract][Full Text] [Related]
13. Evaluation of the chiral recognition properties as well as the column performance of four chiral stationary phases based on cellulose (3,5-dimethylphenylcarbamate) by parallel HPLC and SFC.
Nelander H; Andersson S; Ohlén K
J Chromatogr A; 2011 Dec; 1218(52):9397-405. PubMed ID: 22119140
[TBL] [Abstract][Full Text] [Related]
14. Direct HPLC enantioseparation of chiral aptazepine derivatives on coated and immobilized polysaccharide-based chiral stationary phases.
Cirilli R; Orlando V; Ferretti R; Turchetto L; Silvestri R; De Martino G; La Torre F
Chirality; 2006 Aug; 18(8):621-32. PubMed ID: 16715514
[TBL] [Abstract][Full Text] [Related]
15. Exploring chiral separation of 3-carboxamido-5-aryl isoxazole derivatives by supercritical fluid chromatography on amylose and cellulose tris dimethyl- and chloromethyl phenylcarbamate polysaccharide based stationary phases.
Zehani Y; Lemaire L; Ghinet A; Millet R; Chavatte P; Vaccher C; Lipka E
J Chromatogr A; 2016 Oct; 1467():473-481. PubMed ID: 27452989
[TBL] [Abstract][Full Text] [Related]
16. Enantioseparation of some clinically used drugs by HPLC using cellulose Tris (3,5-dichlorophenylcarbamate) chiral stationary phase.
Ali I; Aboul-Enein HY
Biomed Chromatogr; 2003; 17(2-3):113-7. PubMed ID: 12717799
[TBL] [Abstract][Full Text] [Related]
17. Chromatographic enantioseparation of chiral sulfinamide derivatives on polysaccharide-based chiral stationary phases.
Zeng Q; Wen Q; Xiang Y; Zhang L
J Chromatogr A; 2018 Oct; 1571():240-244. PubMed ID: 30122247
[TBL] [Abstract][Full Text] [Related]
18. Chiral recognition ability and solvent versatility of bonded amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase: enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs.
Ghanem A; Al-Humaidi E
Chirality; 2007 Jun; 19(6):477-84. PubMed ID: 17394130
[TBL] [Abstract][Full Text] [Related]
19. Optimization of Liquid Crystalline Mixtures Enantioseparation on Polysaccharide-Based Chiral Stationary Phases by Reversed-Phase Chiral Liquid Chromatography.
Urbańska M
Int J Mol Sci; 2024 Jun; 25(12):. PubMed ID: 38928182
[TBL] [Abstract][Full Text] [Related]
20. High-performance liquid chromatographic enantioseparation of isopulegol-based ß-amino lactone and ß-amino amide analogs on polysaccharide-based chiral stationary phases focusing on the change of the enantiomer elution order.
Tanács D; Orosz T; Szakonyi Z; Le TM; Fülöp F; Lindner W; Ilisz I; Péter A
J Chromatogr A; 2020 Jun; 1621():461054. PubMed ID: 32204880
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]