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Journal Abstract Search

232 related items for PubMed ID: 27834832

  • 21. Chiral stationary phase based on cellulose derivative coated polymer microspheres and its separation performance.
    Li L, Yuan XT, Shi ZG, Xu LY.
    J Chromatogr A; 2020 Jul 19; 1623():461154. PubMed ID: 32505273
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  • 24. 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 19; 31(3):164-173. PubMed ID: 30633381
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  • 29. Monolithic silica capillary columns with immobilized cellulose tris(3,5-dimethylphenylcarbamate) for enantiomer separations in CEC.
    He C, Hendrickx A, Mangelings D, Smeyers-Verbeke J, Vander Heyden Y.
    Electrophoresis; 2009 Nov 19; 30(22):3796-803. PubMed ID: 19885889
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  • 30. 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 Nov 19; 17(2-3):113-7. PubMed ID: 12717799
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  • 31. A mesoporous silica nanoparticles immobilized open-tubular capillary column with a coating of cellulose tris(3,5-dimethylphenyl-carbamate) for enantioseparation in CEC.
    Dong X, Wu R, Dong J, Wu M, Zhu Y, Zou H.
    Electrophoresis; 2008 Sep 19; 29(18):3933-40. PubMed ID: 18850662
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  • 32. Synthesis of cellulose-2,3-bis(3,5-dimethylphenylcarbamate) in an ionic liquid and its chiral separation efficiency as stationary phase.
    Liu R, Zhang Y, Bai L, Huang M, Chen J, Zhang Y.
    Int J Mol Sci; 2014 Apr 11; 15(4):6161-8. PubMed ID: 24733066
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  • 33. 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 07; 1467():473-481. PubMed ID: 27452989
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  • 34. 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 07; 27(8):518-22. PubMed ID: 26039871
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  • 35. High-performance liquid chromatographic evaluation of a coated cellulose tris(3,5-dimethylphenylcarbamate) chiral stationary phase having a small-pore silica support.
    Liu Y, Zou H.
    J Chromatogr A; 2008 Jan 18; 1178(1-2):118-25. PubMed ID: 18068714
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  • 36. 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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  • 37. High-performance liquid chromatographic enantioseparation of unusual amino acid derivatives with axial chirality on polysaccharide-based chiral stationary phases.
    López-Ram-de-Víu P, Gálvez JA, Díaz-de-Villegas MD.
    J Chromatogr A; 2015 Apr 17; 1390():78-85. PubMed ID: 25748541
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  • 38. [Preparation, characterization and evaluation of cellulose tris (3,5-dimethylphencarbamate) chiral stationary phase].
    Hou JG, Deng QL, Meng XR, Liu HL, Yang W, Mo ZL, Gao JZ.
    Se Pu; 2001 Mar 17; 19(2):154-6. PubMed ID: 12541662
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  • 39. 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 24; 1365():86-93. PubMed ID: 25262030
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  • 40. Insights into chiral recognition mechanisms in supercritical fluid chromatography. II. Factors contributing to enantiomer separation on tris-(3,5-dimethylphenylcarbamate) of amylose and cellulose stationary phases.
    West C, Guenegou G, Zhang Y, Morin-Allory L.
    J Chromatogr A; 2011 Apr 15; 1218(15):2033-57. PubMed ID: 21185024
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