@article{oai:soar-ir.repo.nii.ac.jp:00020834,
 author = {Motoyoshiya, Jiro and Tomioka, Satoshi and Kobayashi, Daigo and Fujimoto, Tetsuya},
 issue = {12},
 journal = {TETRAHEDRON LETTERS},
 month = {Mar},
 note = {Available online 7 February 2018., Synthesis and spectral study of two new cyano-substituted fluorescamine as the fluorescent probes for amino acid detection have been carried out comparing with the original fluorescamine. Of the three compounds, the derivative with a cyano group at the meta-position on the 4-phenyl group was found to be superior to the original one in the reactivity toward some amino acids as well as the fluorescence intensity of the adducts. The fluorescent amino acid adducts were also applied to the peroxyoxalate chemiluminescence system as the fluorophores, in which the derivative described above was found to be more effective also in chemiluminescence than the original one. (C) 2018 Elsevier Ltd. All rights reserved., Article, TETRAHEDRON LETTERS. 59(12):1104-1107 (2018)},
 pages = {1104--1107},
 title = {A new cyano-substituted fluorescamine superior to its original form as a fluorescent probe for amino acid detection},
 volume = {59},
 year = {2018}
}