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499 related items for PubMed ID: 23283776

  • 1. Enantioseparations of primary amino compounds by high-performance liquid chromatography using chiral crown ether-based chiral stationary phase.
    Hyun MH.
    Methods Mol Biol; 2013; 970():165-76. PubMed ID: 23283776
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  • 2. 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
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  • 3. Preparation of a new doubly tethered chiral stationary phase based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid and its application.
    Hyun MH, Song Y, Cho YJ, Kim DH.
    J Chromatogr A; 2006 Mar 10; 1108(2):208-17. PubMed ID: 16445923
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  • 4. 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
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  • 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 30; 17(3):142-8. PubMed ID: 15704196
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  • 7. Unusual resolution of N-(3,5-dinitrobenzoyl)-alpha-amino acids on a chiral stationary phase based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid.
    Hyun MH, Tan G, Xue JY.
    J Chromatogr A; 2005 Dec 02; 1097(1-2):188-91. PubMed ID: 16266713
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  • 11. Effect of the residual silanol group protection on the liquid chromatographic resolution of racemic primary amino compounds on a chiral stationary phase based on optically active (3,3'-diphenyl-1,1'-binaphthyl)-20-crown-6.
    Hyun MH, Han SC, Choi HJ, Kang BS, Ha HJ.
    J Chromatogr A; 2007 Jan 05; 1138(1-2):169-74. PubMed ID: 17084849
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  • 12. 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 05; 32(7):981-7. PubMed ID: 19306252
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  • 17. Development and application of chiral crown ethers as selectors for chiral separation in high-performance liquid chromatography and nuclear magnetic resonance spectroscopy.
    Paik MJ, Kang JS, Huang BS, Carey JR, Lee W.
    J Chromatogr A; 2013 Jan 25; 1274():1-5. PubMed ID: 23290338
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  • 18. Liquid chromatographic resolution of mexiletine and its analogs on crown ether-based chiral stationary phases.
    Jin KB, Kim HE, Hyun MH.
    Chirality; 2014 May 25; 26(5):272-8. PubMed ID: 24677299
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  • 19. Liquid chromatographic resolution of 3-amino-1,4-benzodiazepin-2-ones on crown ether-based chiral stationary phases.
    Park JY, Jin KB, Hyun MH.
    Chirality; 2012 May 25; 24(5):427-31. PubMed ID: 22508444
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