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https://doi.org/10.1002/chem.201200206
Title: | Catalytic and enantioselective α-functionalization of oxindoles through oxidative reactions with naphthoquinones | Authors: | Siau, W.-Y. Li, W. Xue, F. Ren, Q. Wu, M. Sun, S. Guo, H. Jiang, X. Wang, J. |
Keywords: | asymmetric catalysis indane organocatalysis oxindole thiourea |
Issue Date: | 27-Jul-2012 | Citation: | Siau, W.-Y., Li, W., Xue, F., Ren, Q., Wu, M., Sun, S., Guo, H., Jiang, X., Wang, J. (2012-07-27). Catalytic and enantioselective α-functionalization of oxindoles through oxidative reactions with naphthoquinones. Chemistry - A European Journal 18 (31) : 9491-9495. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201200206 | Abstract: | Strong as an oxindole: The enantioselective assembly of 3,3-disubstituted oxindoles is an attractive and valuable target because of the unique properties of the oxindole core. A new organocatalyzed and enantioselective aerobic oxidative strategy for the assembly of this core structure from oxindoles and simple naphthoquinones is reported (see scheme). Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | Source Title: | Chemistry - A European Journal | URI: | http://scholarbank.nus.edu.sg/handle/10635/93233 | ISSN: | 09476539 | DOI: | 10.1002/chem.201200206 |
Appears in Collections: | Staff Publications |
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