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Journal Abstract Search


152 related items for PubMed ID: 27842849

  • 21. Improved preparation of chiral stationary phases via immobilization of polysaccharide derivative-based selectors using diisocyanates.
    Tang S, Liu G, Li X, Jin Z, Wang F, Pan F, Okamoto Y.
    J Sep Sci; 2011 Aug; 34(15):1763-71. PubMed ID: 21688393
    [Abstract] [Full Text] [Related]

  • 22. Performance comparison of chiral separation materials derived from N-cyclohexylcarbonyl and N-hexanoyl chitosans.
    Tang S, Liu JD, Chen W, Huang SH, Zhang J, Bai ZW.
    J Chromatogr A; 2018 Jan 12; 1532():112-123. PubMed ID: 29246422
    [Abstract] [Full Text] [Related]

  • 23. Enantioseparation performance of novel benzimido-β-cyclodextrins derivatized by ionic liquids as chiral stationary phases.
    Li X, Zhou Z.
    Anal Chim Acta; 2014 Mar 28; 819():122-9. PubMed ID: 24636420
    [Abstract] [Full Text] [Related]

  • 24. Chiral separation materials based on derivatives of 6-amino-6-deoxyamylose.
    Gao YY, Zhang YH, Zhang S, Chen W, Bai ZW.
    Chirality; 2021 Dec 28; 33(12):899-914. PubMed ID: 34608664
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. 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 29; 1217(44):6942-55. PubMed ID: 20863505
    [Abstract] [Full Text] [Related]

  • 27. Enantioseparation characteristics of tadalafil and its intermediate on chitin derived chiral stationary phases.
    Zhang J, Wang ZQ, Wang XC, Zhang JJ, Bai ZW, Chen W.
    Analyst; 2015 Aug 21; 140(16):5593-600. PubMed ID: 26115207
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  • 28. Controlled synthesis, immobilization and chiral recognition of carboxylic acid functionalized cellulose tris(3,5-dimethylphenylcarbamate).
    Han M, Jin X, Yang H, Liu X, Liu Y, Ji S.
    Carbohydr Polym; 2017 Sep 15; 172():223-229. PubMed ID: 28606529
    [Abstract] [Full Text] [Related]

  • 29. 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
    [Abstract] [Full Text] [Related]

  • 30. [Preparation and chiral recognition of heterosubstituted amylose derivatives-based chiral stationary phases].
    Wang B, Bao M, Lin S, Ma J, Tang S.
    Se Pu; 2017 Jun 08; 35(6):572-577. PubMed ID: 29048782
    [Abstract] [Full Text] [Related]

  • 31. 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
    [Abstract] [Full Text] [Related]

  • 32. Structure screening and performance restoration of chiral separation materials based on chitosan derivatives.
    Zhang GH, Fu KQ, Xi JB, Chen W, Tang S, Bai ZW.
    Carbohydr Polym; 2019 Jun 15; 214():259-268. PubMed ID: 30925995
    [Abstract] [Full Text] [Related]

  • 33. 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 15; 31(3):164-173. PubMed ID: 30633381
    [Abstract] [Full Text] [Related]

  • 34. Performances comparison of enantiomeric separation materials prepared from shrimp and crab shells.
    Yang F, Cai ML, Chen W, Bai ZW.
    Carbohydr Polym; 2019 Jan 15; 204():238-246. PubMed ID: 30366536
    [Abstract] [Full Text] [Related]

  • 35. Comparison in enantioseparation performance of chiral stationary phases prepared from chitosans of different sources and molecular weights.
    Zhang GH, Xi JB, Chen W, Bai ZW.
    J Chromatogr A; 2020 Jun 21; 1621():461029. PubMed ID: 32192704
    [Abstract] [Full Text] [Related]

  • 36. Synthesis and enantioseparation behaviors of novel immobilized 3,5-dimethylphenylcarbamoylated polysaccharide chiral stationary phases.
    Tan Y, Fan J, Lin C, Tu H, Zheng S, Zhang W.
    J Sep Sci; 2014 Mar 21; 37(5):488-94. PubMed ID: 24376089
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  • 37. Synthesis of dendrimer-type chiral stationary phases based on the selector of (1S,2R)-(+)-2-amino-1,2-diphenylethanol derivate and their enantioseparation evaluation by HPLC.
    He BJ, Yin CQ, Li SR, Bai ZW.
    Chirality; 2010 Jan 21; 22(1):69-76. PubMed ID: 19319988
    [Abstract] [Full Text] [Related]

  • 38. Simultaneous separation and enantioseparation of thalidomide and its hydroxylated metabolites using high-performance liquid chromatography in common-size columns, capillary liquid chromatography and nonaqueous capillary electrochromatography.
    Meyring M, Chankvetadze B, Blaschke G.
    J Chromatogr A; 2000 Apr 21; 876(1-2):157-67. PubMed ID: 10823511
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  • 39. 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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  • 40. Enantioseparation of vesamicol and novel vesamicol analogs by high-performance liquid chromatography on different chiral stationary phases.
    Wenzel B, Fischer S, Brust P, Steinbach J.
    J Chromatogr A; 2010 Jun 11; 1217(24):3855-62. PubMed ID: 20447641
    [Abstract] [Full Text] [Related]


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