176 related articles for article (PubMed ID: 14735977)
1. High-performance liquid chromatographic enantioseparation using chitin carbamate derivatives as chiral stationary phases.
Yamamoto C; Hayashi T; Okamoto Y
J Chromatogr A; 2003 Dec; 1021(1-2):83-91. PubMed ID: 14735977
[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 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]
4. Synthesis of chitosan 3,6-diphenylcarbamate-2-urea derivatives and their applications as chiral stationary phases for high-performance liquid chromatography.
Zhang L; Shen J; Zuo W; Okamoto Y
J Chromatogr A; 2014 Oct; 1365():86-93. PubMed ID: 25262030
[TBL] [Abstract][Full Text] [Related]
5. Enantioseparation using chitosan 2-isopropylthiourea-3,6-dicarbamate derivatives as chiral stationary phases for high-performance liquid chromatography.
Zhang L; Deng H; Wu X; Gao H; Shen J; Cao H; Qiao Y; Okamoto Y
J Chromatogr A; 2020 Jul; 1623():461174. PubMed ID: 32505278
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
8. 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]
9. 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]
10. Enantioseparation characteristics of the chiral stationary phases based on natural and regenerated chitins.
Mei XM; Chen W; Bai ZW
J Sep Sci; 2017 Apr; 40(8):1710-1717. PubMed ID: 28225215
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
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. Quaternized chitin used as chiral stationary phase for HPLC and the high enantioseparation of 1,2,3,4-tetrahydro-1-naphthalenamine racemates.
Pu Y; Shi J; Shi B; Li G; Du Y
Int J Biol Macromol; 2021 Dec; 193(Pt A):809-813. PubMed ID: 34728299
[TBL] [Abstract][Full Text] [Related]
15. Enantioseparation using urea- and imide-bearing chitosan phenylcarbamate derivatives as chiral stationary phases for high-performance liquid chromatography.
Yamamoto C; Fujisawa M; Kamigaito M; Okamoto Y
Chirality; 2008 Mar; 20(3-4):288-94. PubMed ID: 17597117
[TBL] [Abstract][Full Text] [Related]
16. Enantioseparation of the antidepressant reboxetine.
Cannazza G; Braghiroli D; Carrozzo MM; Parenti C; Sabbioni C; Mandrioli R; Fanali S; Raggi MA
J Pharm Biomed Anal; 2008 Nov; 48(3):991-6. PubMed ID: 18707836
[TBL] [Abstract][Full Text] [Related]
17. Preparation and chiral recognition in HPLC of cellulose 3,5-dichlorophenylcarbamates immobilized onto silica gel.
Qu HT; Li JQ; Wu GS; Shen J; Shen XD; Okamoto Y
J Sep Sci; 2011 Mar; 34(5):536-41. PubMed ID: 21280215
[TBL] [Abstract][Full Text] [Related]
18. Enantioseparation using ortho- or meta-substituted phenylcarbamates of amylose as chiral stationary phases for high-performance liquid chromatography.
Shen J; Zhao Y; Inagaki S; Yamamoto C; Shen Y; Liu S; Okamoto Y
J Chromatogr A; 2013 Apr; 1286():41-6. PubMed ID: 23506702
[TBL] [Abstract][Full Text] [Related]
19. The interactions between chiral analytes and chitosan-based chiral stationary phases during enantioseparation.
Chen W; Jiang JZ; Qiu GS; Tang S; Bai ZW
J Chromatogr A; 2021 Aug; 1650():462259. PubMed ID: 34090134
[TBL] [Abstract][Full Text] [Related]
20. Eluent Tolerance and Enantioseparation Recovery of Chiral Packing Materials Based on Chitosan Bis(Phenylcarbamate)-(n-Octyl Urea)s for High Performance Liquid Chromatography.
Wang J; Huang SH; Chen W; Bai ZW
Molecules; 2016 Nov; 21(11):. PubMed ID: 27845761
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]