Diels-Alder reactions of furo [3,4-b] 1,4-benzodioxins : An efficient approach to substituted dibenzo [b,e][1,4] dioxins

Article abstract of DOI:10.1080/00397919608003564

In view of their potential biological properties, different substituted dibenzo [b,e] [1,4] dioxins have been synthesized using Diels-Alder reactions. This required the preparation of furobenzodioxins and further dehydration of the bicyclo-adducts of the cycloaddition.

Full text of DOI:10.1080/00397919608003564

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Synthetic Communications: An
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Diels-Alder Reactions of Furo
[3,4-b] 1,4-benzodioxins:
An Efficient Approach to
Substituted Dibenzo [b,e][1,4]
Dioxins
N. Ruiz a , C. Buon a , M. D. Pujol b , G. Guillaumet a
& G. Coudert a
a Laboratoire de Chimie Bioorganique et Analytique,
URA CNRS 499, Université , d'Orléans, B.P 6759,
45067, Orléans Cedex 2, France
b Laboratorio de Química Farmacéutica, Facultad de
Farmácia, Universidad de Barcelona , Av. Diagonal
643, 08028, Barcelona, (Spain)
Published online: 21 Aug 2006.
To cite this article: N. Ruiz , C. Buon , M. D. Pujol , G. Guillaumet & G. Coudert
(1996) Diels-Alder Reactions of Furo [3,4-b] 1,4-benzodioxins: An Efficient Approach
to Substituted Dibenzo [b,e][1,4] Dioxins, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 26:11, 2057-2066,
DOI: 10.1080/00397919608003564
To link to this article: http://dx.doi.org/10.1080/00397919608003564
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