116 related articles for article (PubMed ID: 35550775)
1. Molecular structure and chiral recognition ability of highly branched cyclic dextrin carbamate derivative.
Kishimoto A; Mizuguchi M; Ryoki A; Terao K
Carbohydr Polym; 2022 Aug; 290():119491. PubMed ID: 35550775
[TBL] [Abstract][Full Text] [Related]
2. Does local chain conformation affect the chiral recognition ability of an amylose derivative? Comparison between linear and cyclic amylose tris(3,5-dimethylphenylcarbamate).
Ryoki A; Kimura Y; Kitamura S; Maeda K; Terao K
J Chromatogr A; 2019 Aug; 1599():144-151. PubMed ID: 31003715
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Structural analysis of amylose tris(3,5-dimethylphenylcarbamate) by NMR relevant to its chiral recognition mechanism in HPLC.
Yamamoto C; Yashima E; Okamoto Y
J Am Chem Soc; 2002 Oct; 124(42):12583-9. PubMed ID: 12381203
[TBL] [Abstract][Full Text] [Related]
5. [Chiral separation of glycerin monosulfides and bisulfides with a stationary phase of amylose-tris(3,5-dimethylphenylcarbamate)].
Yu ZW; Liu X; Jiang SX; Chen LR
Se Pu; 2000 Jan; 18(1):39-41. PubMed ID: 12541452
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Resolution of chiral cannabinoids on amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase: effects of structural features and mobile phase additives.
Levin S; Abu-Lafi S; Zahalka J; Mechoulam R
J Chromatogr A; 1993 Nov; 654(1):53-64. PubMed ID: 8275178
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. A protocol to replace dedication to either normal phase or polar organic mode for chiral stationary phases containing amylose tris(3,5-dimethylphenylcarbamate).
Horváth S; Eke Z; Németh G
J Chromatogr A; 2022 Jun; 1673():463052. PubMed ID: 35490465
[TBL] [Abstract][Full Text] [Related]
10. Enantiomeric resolution of kielcorin derivatives by HPLC on polysaccharide stationary phases using multimodal elution.
Sousa EP; Tiritan ME; Oliveira RV; Afonso CM; Cass QB; Pinto MM
Chirality; 2004 May; 16(5):279-85. PubMed ID: 15069657
[TBL] [Abstract][Full Text] [Related]
11. Effects of backbone and side chain on the molecular environments of chiral cavities in polysaccharide-based biopolymers.
Kasat RB; Wang NH; Franses EI
Biomacromolecules; 2007 May; 8(5):1676-85. PubMed ID: 17439279
[TBL] [Abstract][Full Text] [Related]
12. Enantioselective separation of racemates using CHIRALPAK IG amylose-based chiral stationary phase under normal standard, non-standard and reversed phase high performance liquid chromatography.
Ghanem A; Wang C
J Chromatogr A; 2018 Jan; 1532():89-97. PubMed ID: 29191406
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Solvent-dependent conformation of a regioselective amylose carbamate: amylose-2-acetyl-3,6-bis(phenylcarbamate).
Tsuda M; Terao K; Kitamura S; Sato T
Biopolymers; 2012 Dec; 97(12):1010-7. PubMed ID: 22987591
[TBL] [Abstract][Full Text] [Related]
15. Exploitation of the enantioselectivity space of coated amylose tris(3,5-dimethylphenylcarbamate) in mixtures of 2-propanol and acetonitrile.
Horváth S; Nguyen Thuy HH; Eke Z; Németh G
J Chromatogr A; 2023 Aug; 1705():464161. PubMed ID: 37352691
[TBL] [Abstract][Full Text] [Related]
16. Solvent versatility of immobilized 3,5-dimethylphenylcarbamate of amylose in enantiomeric separations by HPLC.
Zhang T; Kientzy C; Franco P; Ohnishi A; Kagamiharb Y; Kurosawa H
J Chromatogr A; 2005 May; 1075(1-2):65-75. PubMed ID: 15974119
[TBL] [Abstract][Full Text] [Related]
17. Immobilized versus coated amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phases for the enantioselective separation of cyclopropane derivatives by liquid chromatography.
Ghanem A; Naim L
J Chromatogr A; 2006 Jan; 1101(1-2):171-8. PubMed ID: 16246350
[TBL] [Abstract][Full Text] [Related]
18. Hysteresis of retention and enantioselectivity on amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phases in mixtures of 2-propanol and methanol.
Horváth S; Németh G
J Chromatogr A; 2018 Sep; 1568():149-159. PubMed ID: 30064816
[TBL] [Abstract][Full Text] [Related]
19. Synthesis and chiral recognition of novel amylose derivatives containing regioselectively benzoate and phenylcarbamate groups.
Shen J; Ikai T; Okamoto Y
J Chromatogr A; 2010 Feb; 1217(7):1041-7. PubMed ID: 19647833
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
