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|Title:||Catalytic and enantioselective α-functionalization of oxindoles through oxidative reactions with naphthoquinones||Authors:||Siau, W.-Y.
|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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