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Issue 19, 2011
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A highly organocatalytic stereoselective double Michael reaction: efficient construction of optically enriched spirocyclic oxindoles

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Abstract

An effective double Michael reaction has been disclosed to access spirocyclic oxindoles in high yields (up to 98%) and excellent enantioselectivities (up to 98% ee).

Graphical abstract: A highly organocatalytic stereoselective double Michael reaction: efficient construction of optically enriched spirocyclic oxindoles

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Publication details

The article was received on 01 Mar 2011, accepted on 17 Mar 2011 and first published on 01 Apr 2011


Article type: Communication
DOI: 10.1039/C1CC11223F
Citation: Chem. Commun., 2011,47, 5593-5595
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    A highly organocatalytic stereoselective double Michael reaction: efficient construction of optically enriched spirocyclic oxindoles

    L. Wang, L. Peng, J. Bai, L. Jia, X. Luo, Q. Huang, X. Xu and L. Wang, Chem. Commun., 2011, 47, 5593
    DOI: 10.1039/C1CC11223F

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