2024-03-29T08:00:18Z
https://soar-ir.repo.nii.ac.jp/oai
oai:soar-ir.repo.nii.ac.jp:00020834
2022-12-14T04:18:09Z
1309:1310
A new cyano-substituted fluorescamine superior to its original form as a fluorescent probe for amino acid detection
Motoyoshiya, Jiro
Tomioka, Satoshi
Kobayashi, Daigo
Fujimoto, Tetsuya
Fluorescamine
Fluorescent probe
Cyano group
Peroxyoxalate chemiluminescence
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)
journal article
PERGAMON-ELSEVIER SCIENCE LTD
2018-03-21
application/pdf
TETRAHEDRON LETTERS
12
59
1104
1107
0040-4039
AA00861801
https://soar-ir.repo.nii.ac.jp/record/20834/files/Manus._fluorescamine.pdf
eng
10.1016/j.tetlet.2018.02.011
https://doi.org/10.1016/j.tetlet.2018.02.011
© 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/