Ternary enantioselective complexes from alpha-amino acids, 18-crown-6 ether and a macrocyclic xanthone-based receptor

HERNANDEZ, JV; Oliva, AI; Simon, L.; Muniz, FM; Grande, M; Moran, JR

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