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Journal Abstract Search

161 related items for PubMed ID: 35174536

  • 1. Preparation of cellulose derivative bearing bulky 4-(2-benzothienyl)phenylcarbamate substituents as chiral stationary phase for enantioseparation.
    Wang F, Wang Y, Min Y, Li J, Zhang L, Zheng T, Shen J, Okamoto Y.
    Chirality; 2022 May; 34(5):701-710. PubMed ID: 35174536
    [Abstract] [Full Text] [Related]

  • 2. Synthesis of amylose and cellulose derivatives bearing bulky pendants for high-efficient chiral fluorescent sensing.
    Wang F, Wang W, Wang Y, Zheng W, Zheng T, Zhang L, Okamoto Y, Shen J.
    Carbohydr Polym; 2023 Jul 01; 311():120769. PubMed ID: 37028880
    [Abstract] [Full Text] [Related]

  • 3. Synthesis and chiral recognition of amylose derivatives bearing regioselective phenylcarbamate substituents at 2,6- and 3-positions for high-performance liquid chromatography.
    Shen J, Li G, Yang Z, Okamoto Y.
    J Chromatogr A; 2016 Oct 07; 1467():199-205. PubMed ID: 27452988
    [Abstract] [Full Text] [Related]

  • 4. [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 07; 29(11):1087-92. PubMed ID: 22393696
    [Abstract] [Full Text] [Related]

  • 5. 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 19; 1572():54-61. PubMed ID: 30146373
    [Abstract] [Full Text] [Related]

  • 6. 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 08; 21(11):. PubMed ID: 27834832
    [Abstract] [Full Text] [Related]

  • 7. Enantioseparation and molecular modeling study of chiral amines as three naphthaldimine derivatives using amylose or cellulose trisphenylcarbamate chiral stationary phases.
    Adhikari S, Bhujbal S, Paik MJ, Lee W.
    Chirality; 2023 Jan 08; 35(1):29-39. PubMed ID: 36323631
    [Abstract] [Full Text] [Related]

  • 8. 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 12; 1217(7):1041-7. PubMed ID: 19647833
    [Abstract] [Full Text] [Related]

  • 9. 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 19; 1286():41-6. PubMed ID: 23506702
    [Abstract] [Full Text] [Related]

  • 10. Separation of enantiomers of chiral basic drugs with amylose- and cellulose- phenylcarbamate-based chiral columns in acetonitrile and aqueous-acetonitrile in high-performance liquid chromatography with a focus on substituent electron-donor and electron-acceptor effects.
    Matarashvili I, Chelidze A, Dolidze G, Kobidze G, Zaqashvili N, Dadianidze A, Bacskay I, Felinger A, Farkas T, Chankvetadze B.
    J Chromatogr A; 2020 Aug 02; 1624():461218. PubMed ID: 32540066
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. High-performance liquid chromatographic enantioseparation of isopulegol-based ß-amino lactone and ß-amino amide analogs on polysaccharide-based chiral stationary phases focusing on the change of the enantiomer elution order.
    Tanács D, Orosz T, Szakonyi Z, Le TM, Fülöp F, Lindner W, Ilisz I, Péter A.
    J Chromatogr A; 2020 Jun 21; 1621():461054. PubMed ID: 32204880
    [Abstract] [Full Text] [Related]

  • 13. Functionalities tuned enantioselectivity of phenylcarbamate cyclodextrin clicked chiral stationary phases in HPLC.
    Tang J, Lin Y, Yang B, Zhou J, Tang W.
    Chirality; 2017 Sep 21; 29(9):566-573. PubMed ID: 28710781
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 1440():112-122. PubMed ID: 26931425
    [Abstract] [Full Text] [Related]

  • 15. Enantioseparation on helical poly(diphenylacetylene)s bearing optically-active pendants: Effects of differences in higher-order structures of kinetically-trapped and thermodynamically-stable states on chiral recognition ability.
    Hirose D, Ogino K, Uematsu K, Maeda K.
    J Chromatogr A; 2022 Jul 19; 1675():463164. PubMed ID: 35660321
    [Abstract] [Full Text] [Related]

  • 16. Enantioseparation of isoxazolines with functionalized perphenylcarbamate cyclodextrin clicked chiral stationary phases in HPLC.
    Yang B, Zhou J, Wang Y, Tang J, Tang W.
    Electrophoresis; 2017 Aug 19; 38(15):1939-1947. PubMed ID: 28176345
    [Abstract] [Full Text] [Related]

  • 17. High performance liquid chromatographic enantioseparation of chiral bridged polycyclic compounds on chiralcel OD-H and chiralpak OT(+).
    Peluso P, Cossu S, Moretto F, Marchetti M.
    Chirality; 2009 May 19; 21(5):507-18. PubMed ID: 18655168
    [Abstract] [Full Text] [Related]

  • 18. 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 19; 27(8):518-22. PubMed ID: 26039871
    [Abstract] [Full Text] [Related]

  • 19. Influence of the substituents on phenyl groups on enantioseparation property of amylose phenylcarbamates.
    Bi W, Wang F, Han J, Liu B, Shen J, Zhang L, Okamoto Y.
    Carbohydr Polym; 2020 Aug 01; 241():116372. PubMed ID: 32507194
    [Abstract] [Full Text] [Related]

  • 20. Development of Amylose- and β-Cyclodextrin-Based Chiral Fluorescent Sensors Bearing Terthienyl Pendants.
    Ikai T, Yun C, Kojima Y, Suzuki D, Maeda K, Kanoh S.
    Molecules; 2016 Nov 11; 21(11):. PubMed ID: 27845730
    [Abstract] [Full Text] [Related]

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