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150 related items for PubMed ID: 27319166

  • 1. [Separation mechanism of chiral stationary phase based on quinine and crown ether for the direct stereoselective separation of amino acids].
    Wu H, Wang D, Zhao J, Ke Y, Liang X.
    Se Pu; 2016 Jan; 34(1):62-7. PubMed ID: 27319166
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  • 3. 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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  • 4. Mechanistic study on the high-selectivity enantioseparation of amino acids using a chiral crown ether-bonded stationary phase and acidic, highly organic mobile phase by liquid chromatography/time-of-flight mass spectrometry.
    Konya Y, Taniguchi M, Furuno M, Nakano Y, Tanaka N, Fukusaki E.
    J Chromatogr A; 2018 Nov 30; 1578():35-44. PubMed ID: 30340763
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  • 6. 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
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  • 7. 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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  • 8. Determination of chromatographic separation parameters of tryptophan enantiomers on a Chirosil-SCA chiral stationary phase by using the inverse method based on the initial guesses estimated from elution by characteristic point method.
    Lee SY, Park KM, Jo SH, Nam HG, Mun S.
    J Chromatogr A; 2011 Feb 25; 1218(8):1195-202. PubMed ID: 21247581
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  • 9. Development of a chiral stationary phase based on cinchonidine. Comparison with a quinine-based chiral column.
    Keunchkarian S, Grisales JO, Padró JM, Boeris S, Castells CB.
    Chirality; 2012 Jul 25; 24(7):512-8. PubMed ID: 22573362
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  • 10. Studies of a pyridino-crown ether-based chiral stationary phase on the enantioseparation of biogenic chiral aralkylamines and α-amino acid esters by high-performance liquid chromatography.
    Lévai S, Németh T, Fődi T, Kupai J, Tóth T, Huszthy P, Balogh GT.
    J Pharm Biomed Anal; 2015 Nov 10; 115():192-5. PubMed ID: 26218505
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  • 13. Quinine versus carbamoylated quinine-based chiral anion exchangers. A comparison regarding enantioselectivity for N-protected amino acids and other chiral acids.
    Mandl A, Nicoletti L, Lämmerhofer M, Lindner W.
    J Chromatogr A; 1999 Oct 08; 858(1):1-11. PubMed ID: 10544887
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  • 15. 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 08; 32(7):981-7. PubMed ID: 19306252
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  • 16. Separation of racemic 2,4-dinitrophenyl amino acids on 9-O-(phenyloxycarbonyl)quinine-bonded carbon-clad zirconia in reversed-phase liquid chromatography.
    Park JH, Lee JW, Kwon SH, Cha JS, Carr PW, McNeff CV.
    J Chromatogr A; 2004 Oct 01; 1050(2):151-7. PubMed ID: 15508307
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  • 17. New chiral crown ether stationary phase for the liquid chromatographic resolution of alpha-amino acid enantiomers.
    Hyun MH, Han SC, Lipshutz BH, Shin YJ, Welch CJ.
    J Chromatogr A; 2001 Mar 02; 910(2):359-65. PubMed ID: 11261730
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  • 18. A study of tetrapeptide enantiomeric separation on crown ether based chiral stationary phases.
    Upmanis T, Kažoka H, Arsenyan P.
    J Chromatogr A; 2020 Jul 05; 1622():461152. PubMed ID: 32376024
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  • 19. Capillary electrophoretic separation of enantiomers of amino acids and amino acid derivatives using crown ether and cyclodextrin.
    Salami M, Jira T, Otto HH.
    Pharmazie; 2005 Mar 05; 60(3):181-5. PubMed ID: 15801669
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  • 20. Liquid chromatographic direct resolution of beta-amino acids on a doubly tethered chiral stationary phase containing N--H amide linkage based on (+)-(18-crown-6)- 2,3,11,12-tetracarboxylic acid.
    Hyun MH, Song Y, Cho YJ, Choi HJ.
    Chirality; 2008 Mar 05; 20(3-4):325-9. PubMed ID: 17614324
    [Abstract] [Full Text] [Related]

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