Application of fluorescamine XII. Chiroptical properties of fluorescamine condensation compounds with some less common α-amino acids
- 1 January 1980
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 92 (2), 447-451
- https://doi.org/10.1016/0006-291x(80)90353-8
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Chiroptical studies of fluorescamine labeled amino acidsBiochemical and Biophysical Research Communications, 1979
- Chiroptical properties of fluorescamine condensation compounds with amino acid esters in situ. Pyrrolinone chirality ruleBiochemical and Biophysical Research Communications, 1978
- Chiroptical properties of fluorescamine condensation compounds with dipeptides in situBiochemical and Biophysical Research Communications, 1977
- Solvent and substituent effects upon the n .fwdarw. .pi.* transition of aliphatic carboxylic acids and estersThe Journal of Organic Chemistry, 1976
- Chiroptical properties of fluorescamine condensation compounds with α-amino acids in situBiochemical and Biophysical Research Communications, 1976
- Preliminary Evalution of Fluorscamine As a Clorimetric Reagent for Primary AminesAnalytical Letters, 1974
- Novel reagent for the fluorometric assay of primary aminesJournal of the American Chemical Society, 1972
- HYDROGEN ELECTRODE POTENTIALS OF PHTHALATE, PHOSPHATE, AND BORATE BUFFER MIXTURESPublished by Elsevier ,1916