Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/22832
Title: Asymmetric vinylogous michael addition/cyclization cascade reaction for the construction of diversely structured spiro-oxindole skeletons
Authors: Shi, XM
Dong, WP
Zhu, LP
Jiang, XX
Wang, R
Keywords: Asymmetric catalysis
Cascade reactions
Dicyanoalkenes
Michael addition
Organocatalysis
Issue Date: 2013
Publisher: Wiley-VCH
Source: Advanced synthesis & catalysis, 2013, v. 355, no. 16, p. 3119-3123 How to cite?
Journal: Advanced synthesis & catalysis 
Abstract: We present the first organocatalytic asymmetric vinylogous Michael/cyclization reaction of α,α-dicyanoalkenes with 3-alkylideneoxindoles. A series of diversely structured spiro-oxindole skeletons was smoothly delivered with excellent yields and stereoselectivity control (94-99% yields, >20:1 dr and 91 to >99% ee).
URI: http://hdl.handle.net/10397/22832
ISSN: 1615-4150
EISSN: 1615-4169
DOI: 10.1002/adsc.201300329
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