Please use this identifier to cite or link to this item: https://doi.org/10.1002/chem.201002202
Title: Enantioselective synthesis of coumarins catalyzed by a bifunctional amine-thiourea catalyst
Authors: Gao, Y.
Ren, Q.
Wang, L. 
Wang, J. 
Keywords: asymmetric catalysis
coumarins
Michael addition
organocatalysis
thioureas
Issue Date: 22-Nov-2010
Citation: Gao, Y., Ren, Q., Wang, L., Wang, J. (2010-11-22). Enantioselective synthesis of coumarins catalyzed by a bifunctional amine-thiourea catalyst. Chemistry - A European Journal 16 (44) : 13068-13071. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201002202
Abstract: Efficient excess: An efficient and facile enantioselective Michael addition reaction through hydrogen-bonding catalysis for the synthesis of coumarin complexes has been developed (see scheme). A simple bifunctional amine-thiourea small molecule has been discovered to catalyze this process with high yields and high to excellent enantiomeric excesses. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Source Title: Chemistry - A European Journal
URI: http://scholarbank.nus.edu.sg/handle/10635/76110
ISSN: 09476539
DOI: 10.1002/chem.201002202
Appears in Collections:Staff Publications

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