Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol402579x
Title: A facile approach for the asymmetric synthesis of oxindoles with a 3-sulfenyl-substituted quaternary stereocenter
Authors: Dou, X.
Zhou, B.
Yao, W.
Zhong, F.
Jiang, C.
Lu, Y. 
Issue Date: 4-Oct-2013
Citation: Dou, X., Zhou, B., Yao, W., Zhong, F., Jiang, C., Lu, Y. (2013-10-04). A facile approach for the asymmetric synthesis of oxindoles with a 3-sulfenyl-substituted quaternary stereocenter. Organic Letters 15 (19) : 4920-4923. ScholarBank@NUS Repository. https://doi.org/10.1021/ol402579x
Abstract: With the employment of a threonine-incorporating multifunctional catalyst 9, Michael addition of 3-sulfenyloxindoles to nitroolefins proceeded stereoselectively, leading to the formation of oxindoles with a 3-sulfenyl-substituted quaternary center in excellent yields, and with high diastereoselectivities and excellent enantioselectivities. © 2013 American Chemical Society.
Source Title: Organic Letters
URI: http://scholarbank.nus.edu.sg/handle/10635/75410
ISSN: 15237060
DOI: 10.1021/ol402579x
Appears in Collections:Staff Publications

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