The Use of Calixarenes in Asymmetric Catalysis

Author(s): Zheng-Yi Li, Jia-Wen Chen, Ying Liu, Wei Xia, Leyong Wang

Journal Name: Current Organic Chemistry

Volume 15 , Issue 1 , 2011

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The use of calixarenes in asymmetric catalysis was described. The current progress of asymmetric catalysts based on calixarene scaffold for the enantioselective reactions including allylation, alkylation, addition of diethylzinc to benzaldehyde, Micheal-type addition, aldol reaction, hydrogenation, Friedal Crafts reaction, epoxidation, hydroformylation, and Biginelli reaction was illustrated. In these cases, calixarenes were used as organocatalysts or ligands in metal-catalyzed asymmetric reactions.

Keywords: Calixarene, Asymmetric catalysis, Supramolecular catalyst, enantioselective reactions, allylation, diethylzinc, benzaldehyde, Micheal-type, aldol reaction, hydrogenation, Friedal Crafts reaction, epoxidation, hydroformylation, Biginelli reaction, calixarenes, organocatalysts, diphosphines, palladium complex, enantioselectivity, triisopropylbenzenesulfonate (Otrips), toyl, benzyl carbonate, tetramethoxyresorcinarene, ammonium thiolate complex, binaphthyl groups, Ti-catalytic site, organocatalyst, hydroxyprolinamide moieties, L-Proline, L-hydroxyproline, interaction, regioselectivity, allylbenzylether, Friedel-Crafts reaction, thiophenol

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Article Details

Year: 2011
Page: [39 - 61]
Pages: 23
DOI: 10.2174/138527211793797837

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