Dienediolates of unsaturated carboxylic acids in synthesis. Tandem Michael-Dieckmann synthesis of substituted 2-cyclohexenones

Article abstract of DOI:10.1080/00397919108021772

3,5-Disubstituted 2-Cyclohexenones are prepared by tandem Michael-Diekcmann addition of lithium dienediolates of dimethylacrylic and β-methylcinnamic acids to lithium carboxylates of unsaturated carboxylic acids.

Full text of DOI:10.1080/00397919108021772

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Dienediolates of Unsaturated
Carboxylic Acids in
Synthesis. Tandem
Michael Diechmann
Synthesis of Substituted 2-
Cyclohexenones
M. J. Aurell a , P. Gaviña a , S. Gil a , A.
Tortajada a & R. Mestres a
a Departament de Quimica Orgànica, Facultat
de Quimica , Universitat de València , Burjassot,
València, Spain
Published online: 23 Sep 2006.
To cite this article: M. J. Aurell , P. Gaviña , S. Gil , A. Tortajada & R. Mestres
(1991) Dienediolates of Unsaturated Carboxylic Acids in Synthesis. Tandem
Michael Diechmann Synthesis of Substituted 2-Cyclohexenones, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 21:18-19, 1825-1831, DOI: 10.1080/00397919108021772
To link to this article: http://dx.doi.org/10.1080/00397919108021772
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