Similar articles

• Chiroptical properties of fluorescamine condensation compounds with secondary amino acids in situ.

  Toome V, Wegrzynski B, Dell J. Toome V, et al. Biochem Biophys Res Commun. 1976 Jul 26;71(2):598-602. doi: 10.1016/0006-291x(76)90829-9. Biochem Biophys Res Commun. 1976. PMID: 9082 No abstract available.
• Colorimetic amino acid analysis using fluorescamine.

  Felix AM, Toome V, De Bernardo S, Weigele M. Felix AM, et al. Arch Biochem Biophys. 1975 Jun;168(2):601-8. doi: 10.1016/0003-9861(75)90292-1. Arch Biochem Biophys. 1975. PMID: 1137411 No abstract available.
• Application of fluorescamine XII. Chiroptical properties of fluorescamine condensation compounds with some less common alpha-amino acids.

  Toome V, Wegrzynski B. Toome V, et al. Biochem Biophys Res Commun. 1980 Jan 29;92(2):447-51. doi: 10.1016/0006-291x(80)90353-8. Biochem Biophys Res Commun. 1980. PMID: 7356476 No abstract available.
• Characterization of selected fluorescamine-amino acid reaction products by high-performance liquid chromatography.

  McHugh W, Sandmann RA, Haney WG. McHugh W, et al. J Chromatogr. 1976 Sep 15;124(2):376-80. doi: 10.1016/s0021-9673(00)89756-3. J Chromatogr. 1976. PMID: 965469 No abstract available.
• Chiroptical properties of fluorescamine condensation compounds with amino acid esters in situ. Pyrrolinone chirality rule.

  Toome V, Wegrzynski B. Toome V, et al. Biochem Biophys Res Commun. 1978 Dec 29;85(4):1496-502. doi: 10.1016/0006-291x(78)91172-5. Biochem Biophys Res Commun. 1978. PMID: 743312 No abstract available.