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Enantioselective fluorescent sensor for amino acid derivatives based on BINOL bearing hexahydropyrrolo[1,2-c]imidazol-1-one units.

Authors :
Wu, Xiaoxia
Xie, Mingsheng
Zhao, Xiaohu
Liu, Xiaohua
Lin, Lili
Feng, Xiaoming
Source :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Jun2014, Vol. 55 Issue 23, p3446-3449. 4p.
Publication Year :
2014

Abstract

Abstract: A chiral fluorescent sensor (Ra,S,l)-3 incorporating (R)-BINOL and l-prolinamide is found efficient in enantioselective recognition of N-Cbz-protected phenylglycine. It is observed that one enantiomer of N-Cbz-protected phenylglycine can obviously increase the fluorescence intensity of (Ra,S,l)-3, while the other enantiomer does not cause much fluorescence enhancement. Such highly enantioselective response makes the sensor (Ra,S,l)-3 useful for the enantioselective fluorescence recognition of other N-Cbz-protected amino acids. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00404039
Volume :
55
Issue :
23
Database :
Academic Search Index
Journal :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :
Academic Journal
Accession number :
96231851
Full Text :
https://doi.org/10.1016/j.tetlet.2014.04.075