Ternary enantioselective complexes from alpha-amino acids, 18-crown-6 ether and a macrocyclic xanthone-based receptor
Abstract
A macrocyclic receptor shaped by two xanthone units bonded to binaphthyl is able to extract zwitterionic amino acids enantioselectively front water to chloroform in the presence of 18-crown-6 ether. Based on H-1 NMR and circular dichroism spectra. the most stable associate of receptor 1 with alanine is assigned to the (M,S) configuration while the opposite configuration in phenylglycine yields the strong associate (M,R). (C) 2004 Elsevier Ltd. All rights reserved.
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| Título según WOS: | ID WOS:000221936100003 Not found in local WOS DB |
| Título de la Revista: | TETRAHEDRON LETTERS |
| Volumen: | 45 |
| Número: | 25 |
| Editorial: | PERGAMON-ELSEVIER SCIENCE LTD |
| Fecha de publicación: | 2004 |
| Página de inicio: | 4831 |
| Página final: | 4833 |
| DOI: |
10.1016/j.tetlet.2004.04.168 |
| Notas: | ISI |