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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 26, 1996 - Issue 11
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Original Articles

Diels-Alder Reactions of Furo [3,4-b] 1,4-benzodioxins: An Efficient Approach to Substituted Dibenzo [b,e][1,4] Dioxins

N. Ruiz Laboratoire de Chimie Bioorganique et Analytique, URA CNRS 499, Université, d'Orléans, B.P 6759, 45067, Orléans Cedex 2, France
,
C. Buon Laboratoire de Chimie Bioorganique et Analytique, URA CNRS 499, Université, d'Orléans, B.P 6759, 45067, Orléans Cedex 2, France
,
M. D. Pujol Laboratorio de Química Farmacéutica, Facultad de Farmácia, Universidad de Barcelona, Av. Diagonal 643, 08028, Barcelona, (Spain)
,
G. Guillaumet Laboratoire de Chimie Bioorganique et Analytique, URA CNRS 499, Université, d'Orléans, B.P 6759, 45067, Orléans Cedex 2, France
&
G. Coudert Laboratoire de Chimie Bioorganique et Analytique, URA CNRS 499, Université, d'Orléans, B.P 6759, 45067, Orléans Cedex 2, France
Pages 2057-2066 | Received 04 Oct 1995, Published online: 21 Aug 2006
 
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Abstract

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.

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