Synthesis, extraction ability and application in asymmetric synthesis of azacrown ethers derived from D-glucose

Article abstract of DOI:10.1016/S0040-4020(98)00938-7

A number of new chiral monoaza-15-crown-5 derivatives (4-9) and lariat ethers (10-15) anellated to phenyl-β-D-glucopyranoside have been synthesized. Their extracting ability was measured with alkali metal (Li, Na, K) and ammonium cations. The derivatives show significant asymmetric induction as phase transfer catalysts in the Michael addition of 2- nitropropane to chalcone (82% ee) although in low yield, and in the Darzens condensation of phenacyl chloride with benzaldehyde (74% ee). The substituent at the nitrogen atom of the crown ethers has a major influence on both the extraction ability and the enantioselectivity.