Microwave-mediated domino reactions in dry medium. Preparation of dihydropyridinones and pyridinones structurally related to Hantzsch esters

Article abstract of DOI:10.1080/00397919708007288

Microwave irradiation of mixtures of 4-arylmethylene-2-phenyloxazol-5(4H)-ones and enaminocarbonyl compounds, in the absence of solvent, affords dihydropyridinone derivatives in quantitative yields. From 4-ethoxymethylene-2-phenyloxazol-5(4H)one and enami

Full text of DOI:10.1080/00397919708007288

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Microwave-Mediated
Domino Reactions in Dry
Medium. Preparation of
Dihydropyridinones and
Pyridinones Structurally
Related to Hantzsch Esters.
Jean Jacques Vanden Eynde a , Nadège Labuche a &
Yves Van Haverbeke a
a University of Mons-Hainaut, Organic Chemistry
department , Place du Parc 20, B-7000, Mons,
Belgium
Published online: 22 Aug 2006.
To cite this article: Jean Jacques Vanden Eynde , Nadège Labuche & Yves Van
Haverbeke (1997) Microwave-Mediated Domino Reactions in Dry Medium. Preparation
of Dihydropyridinones and Pyridinones Structurally Related to Hantzsch Esters.,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 27:21, 3683-3690, DOI: 10.1080/00397919708007288
To link to this article: http://dx.doi.org/10.1080/00397919708007288
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