Please use this identifier to cite or link to this item: 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
Source: 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/10635/75698
ISSN: 09476539
DOI: 10.1002/chem.201200206
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