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Journal Abstract Search

280 related items for PubMed ID: 25477392

  • 1. A novel method for the preparation of a chiral stationary phase containing an enantiopure acridino-18-crown-6 ether selector.
    Németh T, Lévai S, Fődi T, Kupai J, Túrós G, Tóth T, Huszthy P, Balogh GT.
    J Chromatogr Sci; 2015 Mar; 53(3):431-5. PubMed ID: 25477392
    [Abstract] [Full Text] [Related]

  • 2. Enantioseparations of primary amino compounds by high-performance liquid chromatography using chiral crown ether-based chiral stationary phase.
    Hyun MH.
    Methods Mol Biol; 2013 Mar; 970():165-76. PubMed ID: 23283776
    [Abstract] [Full Text] [Related]

  • 3. Synthesis and pKa determination of new enantiopure dimethyl-substituted acridino-crown ethers containing a carboxyl group: Useful candidates for enantiomeric recognition studies.
    Németh T, Dargó G, Petró JL, Petrik Z, Lévai S, Krámos B, Béni Z, Nagy J, Balogh GT, Huszthy P, Tóth T.
    Chirality; 2017 Sep; 29(9):522-535. PubMed ID: 28649773
    [Abstract] [Full Text] [Related]

  • 4. Preparation and evaluation of a chiral stationary phase covalently bound with a chiral pseudo-18-crown-6 ether having a phenolic hydroxy group for enantiomer separation of amino compounds.
    Yongzhu J, Hirose K, Nakamura T, Nishioka R, Ueshige T, Tobe Y.
    J Chromatogr A; 2006 Oct 06; 1129(2):201-7. PubMed ID: 16872621
    [Abstract] [Full Text] [Related]

  • 5. Chiral stationary phase covalently bound with a chiral pseudo-18-crown-6 ether for enantiomer separation of amino compounds using a normal mobile phase.
    Hirose K, Yongzhu J, Nakamura T, Nishioka R, Ueshige T, Tobe Y.
    Chirality; 2005 Mar 06; 17(3):142-8. PubMed ID: 15704196
    [Abstract] [Full Text] [Related]

  • 6. HPLC enantioseparation of beta2-homoamino acids using crown ether-based chiral stationary phase.
    Berkecz R, Ilisz I, Misicka A, Tymecka D, Fülöp F, Choi HJ, Hyun MH, Péter A.
    J Sep Sci; 2009 Apr 06; 32(7):981-7. PubMed ID: 19306252
    [Abstract] [Full Text] [Related]

  • 7. Preparation of Two New Diasteromeric Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid and (R)- or (S)-1-(1-Naphthyl)ethylamine and Chiral Tethering Group Effect on the Chiral Recognition.
    Agneeswari R, Sung JY, Jo ES, Jeon HY, Tamilavan V, Hyun MH.
    Molecules; 2016 Aug 12; 21(8):. PubMed ID: 27529205
    [Abstract] [Full Text] [Related]

  • 8. Liquid chromatographic resolution of mexiletine and its analogs on crown ether-based chiral stationary phases.
    Jin KB, Kim HE, Hyun MH.
    Chirality; 2014 May 12; 26(5):272-8. PubMed ID: 24677299
    [Abstract] [Full Text] [Related]

  • 9. Preparation and studies of chiral stationary phases containing enantiopure acridino-18-crown-6 ether selectors.
    Németh T, Lévai S, Kormos A, Kupai J, Tóth T, Balogh GT, Huszthy P.
    Chirality; 2014 Oct 12; 26(10):651-4. PubMed ID: 25065877
    [Abstract] [Full Text] [Related]

  • 10. Preparation and evaluation of a chiral stationary phase covalently bound with chiral pseudo-1 8-crown-6 ether having 1-phenyl-1,2-cyclohexanediol as a chiral unit.
    Hirose K, Yongzhu J, Nakamura T, Nishioka R, Ueshige T, Tobe Y.
    J Chromatogr A; 2005 Jun 17; 1078(1-2):35-41. PubMed ID: 16007979
    [Abstract] [Full Text] [Related]

  • 11. Preparation and evaluation of novel chiral stationary phases based on quinine derivatives comprising crown ether moieties.
    Wang D, Zhao J, Wu H, Wu H, Cai J, Ke Y, Liang X.
    J Sep Sci; 2015 Jan 17; 38(2):205-10. PubMed ID: 25363571
    [Abstract] [Full Text] [Related]

  • 12. High-performance liquid chromatographic enantioseparation of beta-amino acid stereoisomers on a (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid-based chiral stationary phase.
    Berkecz R, Sztojkov-Ivanov A, Ilisz I, Forró E, Fülöp F, Hyun MH, Péter A.
    J Chromatogr A; 2006 Aug 25; 1125(1):138-43. PubMed ID: 16843474
    [Abstract] [Full Text] [Related]

  • 13. Development of HPLC Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid and Their Applications.
    Hyun MH.
    Chirality; 2015 Sep 25; 27(9):576-88. PubMed ID: 26237013
    [Abstract] [Full Text] [Related]

  • 14. Preparation of a new crown ether-based chiral stationary phase containing thioester linkage for the liquid chromatographic separation of enantiomers.
    Cho HS, Choi HJ, Hyun MH.
    J Chromatogr A; 2009 Oct 30; 1216(44):7446-9. PubMed ID: 19406408
    [Abstract] [Full Text] [Related]

  • 15. High-performance liquid chromatographic enantioseparation of beta-3-homo-amino acid stereoisomers on a (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid-based chiral stationary phase.
    Berkecz R, Ilisz I, Fülöp F, Pataj Z, Hyun MH, Péter A.
    J Chromatogr A; 2008 May 02; 1189(1-2):285-91. PubMed ID: 17936769
    [Abstract] [Full Text] [Related]

  • 16. Unusual enantiomeric separation due to residual amines in chiral crown ether stationary phase linked by long alkyl chain.
    Sung JY, Jin SM, Lee S, An SY, Jin JS.
    Talanta; 2021 Dec 01; 235():122739. PubMed ID: 34517607
    [Abstract] [Full Text] [Related]

  • 17. Comparison of polarimetry and crown ether-based HPLC chiral stationary phase method to determine (L)-amino acid optical purity.
    Lee MS, Khan FN, Shin SC, Jeong ED, Kim HG, Kim MJ, Cho YJ, Cha JY, Hyun MH, Jin JS.
    Food Chem; 2012 Nov 15; 135(2):343-7. PubMed ID: 22868097
    [Abstract] [Full Text] [Related]

  • 18. Preparation and application of HPLC chiral stationary phases based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid.
    Hyun MH.
    J Sep Sci; 2006 Apr 15; 29(6):750-61. PubMed ID: 16830487
    [Abstract] [Full Text] [Related]

  • 19. Noncovalent interactions between ([18]crown-6)-tetracarboxylic acid and amino acids: electrospray-ionization mass spectrometry investigation of the chiral-recognition processes.
    Gerbaux P, De Winter J, Cornil D, Ravicini K, Pesesse G, Cornil J, Flammang R.
    Chemistry; 2008 Apr 15; 14(35):11039-49. PubMed ID: 18956399
    [Abstract] [Full Text] [Related]

  • 20. High-performance liquid chromatographic enantioseparation of beta(2)-amino acids using a long-tethered (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid-based chiral stationary phase.
    Ilisz I, Pataj Z, Berkecz R, Misicka A, Tymecka D, Fülöp F, Choi HJ, Hyun MH, Péter A.
    J Chromatogr A; 2010 Feb 12; 1217(7):1075-82. PubMed ID: 19616782
    [Abstract] [Full Text] [Related]

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