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|Title:||Enantioselective synthesis of coumarins catalyzed by a bifunctional amine-thiourea catalyst||Authors:||Gao, Y.
|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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