Abstract
Two novel types of chiral calix[4]arenes containing hydrazide and dansyl groups were synthesized and examined for their enantioselective recognition abilities by the fluorescence and 1H NMR spectra in CHCl3. The results indicate that both 4a and 4b have excellent enantioselectivities to the N-protected alanine or phenylalanine anions.
| Original language | English |
|---|---|
| Pages (from-to) | 1527-1534 |
| Number of pages | 8 |
| Journal | Tetrahedron Asymmetry |
| Volume | 16 |
| Issue number | 8 |
| DOIs | |
| State | Published - 18 Apr 2005 |
| Externally published | Yes |