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Journal Abstract Search

163 related items for PubMed ID: 36323631

  • 1. 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; 35(1):29-39. PubMed ID: 36323631
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. [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 13; 29(11):1087-92. PubMed ID: 22393696
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  • 4. Enantioseparation of lysine derivatives on amylose tris (3, 5-dimethylphenylcarbamate) as chiral stationary phase with high separation factor.
    Yang Y, Hu J, Fang H, Hou X, Hou Z, Sang L, Yang X.
    J Chromatogr A; 2020 Nov 22; 1632():461598. PubMed ID: 33038752
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  • 5. 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
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  • 6. 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
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  • 7. 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
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  • 9. Preparation and Enantioseparation of Biselector Chiral Stationary Phases Based on Amylose and Chitin Derivatives.
    Zhang J, Wang ZQ, Chen W, Bai ZW.
    Anal Sci; 2015 Oct 07; 31(10):1091-7. PubMed ID: 26460376
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  • 14. Preparation and evaluation of regioselectively substituted amylose derivatives for chiral separations.
    Tang S, Jin Z, Sun B, Wang F, Tang W.
    Chirality; 2017 Sep 07; 29(9):512-521. PubMed ID: 28635058
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  • 15. Enantioseparation of selected chiral sulfoxides using polysaccharide-type chiral stationary phases and polar organic, polar aqueous-organic and normal-phase eluents.
    Chankvetadze B, Yamamoto C, Okamoto Y.
    J Chromatogr A; 2001 Jul 13; 922(1-2):127-37. PubMed ID: 11486857
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  • 16. 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
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  • 19. 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
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