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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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