Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5270145 | Tetrahedron Letters | 2014 | 4 Pages |
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.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xiaoxia Wu, Mingsheng Xie, Xiaohu Zhao, Xiaohua Liu, Lili Lin, Xiaoming Feng,