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Journal Abstract Search

196 related items for PubMed ID: 21737363

  • 1. Use of Marfey's reagent and analogs for chiral amino acid analysis: assessment and applications to natural products and biological systems.
    Bhushan R, Brückner H.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2011 Nov 01; 879(29):3148-61. PubMed ID: 21737363
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  • 4. Reversed-phase high performance liquid chromatographic separation of diastereomers of beta-amino alcohols and microwave assisted synthesis of Marfey's reagent, its chiral variants and diastereomers.
    Bhushan R, Kumar R.
    J Chromatogr A; 2009 Mar 20; 1216(12):2592-6. PubMed ID: 19195660
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  • 5. Reversed-phase liquid chromatographic determination of enantiomers of atenolol in rat plasma using derivatization with Marfey's reagent.
    Bhushan R, Tanwar S.
    Biomed Chromatogr; 2009 Jul 20; 23(7):787-91. PubMed ID: 19309763
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  • 6. Assessment and application of Marfey's reagent and analogs in enantioseparation: a decade's perspective.
    Sethi S, Martens J, Bhushan R.
    Biomed Chromatogr; 2021 Jan 20; 35(1):e4990. PubMed ID: 32959901
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  • 7. Indirect resolution of enantiomers of penicillamine by TLC and HPLC using Marfey's reagent and its variants.
    Bhushan R, Brückner H, Kumar V.
    Biomed Chromatogr; 2007 Oct 20; 21(10):1064-8. PubMed ID: 17516470
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  • 12. C3 and 2D C3 Marfey's Methods for Amino Acid Analysis in Natural Products.
    Vijayasarathy S, Prasad P, Fremlin LJ, Ratnayake R, Salim AA, Khalil Z, Capon RJ.
    J Nat Prod; 2016 Feb 26; 79(2):421-7. PubMed ID: 26863178
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  • 17. Use of Marfey's reagent to quantitate racemization upon anchoring of amino acids to solid supports for peptide synthesis.
    Adamson JG, Hoang T, Crivici A, Lajoie GA.
    Anal Biochem; 1992 Apr 26; 202(1):210-4. PubMed ID: 1621983
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  • 19. A universal HPLC-MS method to determine the stereochemistry of common and unusual amino acids.
    Hess S.
    Methods Mol Biol; 2012 Apr 26; 828():63-75. PubMed ID: 22125137
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  • 20. A liquid chromatography-tandem mass spectrometry assay for Marfey's derivatives of L-Ala, D-Ala, and D-Ala-D-Ala: application to the in vivo confirmation of alanine racemase as the target of cycloserine in Escherichia coli.
    Jamindar D, Gutheil WG.
    Anal Biochem; 2010 Jan 01; 396(1):1-7. PubMed ID: 19748470
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