Cinchona alkaloid-based polymer-bound phase-transfer catalysts: efficient enantioselective alkylation of benzophenone imine of glycine esters.
Baptiste Thierry, Jean-Christophe Plaquevent, Dominique Cahard
Index: Mol. Divers. 9(4) , 277-90, (2005)
Full Text: HTML
Abstract
Cross-linked polystyrene-bound and poly(ethylene glycol)-bound phase-transfer catalysts as well as homopolymers of cinchona alkaloid derivatives have been synthesised. Both soluble and insoluble polymers have been investigated. The enantioselective alkylation of N-diphenyl methylene glycine t-butyl ester has been successfully carried out in heterogeneous and homogeneous systems. High enantioselectivities (up to 96%) have been obtained. The polymer-bound catalysts have been easily recovered and conditions for efficient recycling have been studied.
Related Compounds
Related Articles:
2015-03-11
[Adv. Healthc. Mater. 4(4) , 569-75, (2015)]
1998-09-29
[Biochemistry 37(39) , 13507-15, (1998)]
2001-10-18
[Org. Lett. 3(21) , 3329-31, (2001)]
1984-01-01
[Arzneimittelforschung 34(6) , 687-90, (1984)]
2011-02-07
[Chem. Commun. (Camb.) 47(5) , 1631-3, (2011)]