Calix[4]arene based α-aminophosphonates: Novel carriers for Zwitterionic amino acids transport

Abstract

A series of calix[4]arene based α-aminophosphonates were synthesized by the Kabachnik-Fields reaction of the calixarene-diamine (either at lower or upper rim), diethyl phosphite and a carbonyl compound (acetone or cyclohexanone). These compounds exhibited remarkable selectivity as carriers for the membrane transport of the zwitterionic form of aromatic amino acids.