A facile approach for the asymmetric synthesis of oxindoles with a 3-sulfenyl-substituted quaternary stereocenter

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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