Diels-Alder Reactions of Furo [3,4-b] 1,4-benzodioxins: An Efficient Approach to Substituted Dibenzo [b,e][1,4] Dioxins
- 1 June 1996
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 26 (11) , 2057-2066
- https://doi.org/10.1080/00397919608003564
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.Keywords
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