An intriguing case of the retro-Michael reaction

Article abstract of DOI:10.1080/00397919508013860

In the course of Michael addition of carbanions, derived from malononitrile or cyanoacetic ester, to a nitrostyrol retro reaction has also been observed. Depending on the reaction conditions any of the two compounds formed can be obtained as main product.

Full text of DOI:10.1080/00397919508013860

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Synthetic Communications: An
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Organic Chemistry
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An Intriguing Case of the Retro-
Michael Reaction
Mária Incze a , Gábor Dörnyei a , Mária Kajtár-Peredy
a & Csaba Szántay a
a Central Research Institute for Chemistry Hungarian
Academy of Sciences , PO. Box 17, H-1525,
Budapest, Hungary
Published online: 23 Sep 2006.
To cite this article: Mária Incze , Gábor Dörnyei , Mária Kajtár-Peredy & Csaba
Szántay (1995) An Intriguing Case of the Retro-Michael Reaction, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 25:21, 3389-3393, DOI: 10.1080/00397919508013860
To link to this article: http://dx.doi.org/10.1080/00397919508013860
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