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Journal Abstract Search

234 related items for PubMed ID: 27999329

  • 21.
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  • 22. 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 19; 1623():461174. PubMed ID: 32505278
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  • 23.
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  • 24. 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 14; 46(5):882-91. PubMed ID: 17658716
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  • 27. 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 13; 1346():57-68. PubMed ID: 24792697
    [Abstract] [Full Text] [Related]

  • 28. 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 20; 1321():38-47. PubMed ID: 24231262
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  • 29. 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 03; 1104(1-2):62-8. PubMed ID: 16359692
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  • 32. Evaluation of novel amylose and cellulose-based chiral stationary phases for the stereoisomer separation of flavanones by means of nano-liquid chromatography.
    Si-Ahmed K, Aturki Z, Chankvetadze B, Fanali S.
    Anal Chim Acta; 2012 Aug 13; 738():85-94. PubMed ID: 22790704
    [Abstract] [Full Text] [Related]

  • 33. 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 13; 19(6):477-84. PubMed ID: 17394130
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  • 34. Comparative study on retention behaviour and enantioresolution of basic and neutral structurally unrelated compounds with cellulose-based chiral stationary phases in reversed phase liquid chromatography-mass spectrometry conditions.
    Pérez-Baeza M, Escuder-Gilabert L, Martín-Biosca Y, Sagrado S, Medina-Hernández MJ.
    J Chromatogr A; 2022 Jun 21; 1673():463073. PubMed ID: 35500389
    [Abstract] [Full Text] [Related]

  • 35. The comparison in enantioseparation ability of the chiral stationary phases with single and mixed selector--the selectors derived from two D-tartrates.
    Chen J, Li MZ, Xiao YH, Chen W, Li SR, Bai ZW.
    Chirality; 2011 Mar 21; 23(3):228-36. PubMed ID: 20882599
    [Abstract] [Full Text] [Related]

  • 36. From analytical methods to large scale chiral supercritical fluid chromatography using chlorinated chiral stationary phases.
    Wu DR, Yip SH, Li P, Sun D, Mathur A.
    J Chromatogr A; 2016 Feb 05; 1432():122-31. PubMed ID: 26768405
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  • 37.
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  • 38. Impact of immobilized polysaccharide chiral stationary phases on enantiomeric separations.
    Ali I, Aboul-Enein HY.
    J Sep Sci; 2006 Apr 05; 29(6):762-9. PubMed ID: 16830488
    [Abstract] [Full Text] [Related]

  • 39. Enantioseparations of primary amino compounds by high-performance liquid chromatography using chiral crown ether-based chiral stationary phase.
    Hyun MH.
    Methods Mol Biol; 2013 Apr 05; 970():165-76. PubMed ID: 23283776
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  • 40.
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