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.
Más información
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 |