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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
Synthetic Communications ( IF 1.8 ) Pub Date : 1996-06-01 , DOI: 10.1080/00397919608003564
N. Ruiz , C. Buon , M. D. Pujol , G. Guillaumet , G. Coudert

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.

中文翻译:

Furo [3,4-b] 1,4-苯并二恶英的 Diels-Alder 反应:取代二苯并 [b,e][1,4] 二恶英的有效方法

摘要 鉴于其潜在的生物学特性,已使用 Diels-Alder 反应合成了不同的取代二苯并 [b,e][1,4] 二恶英。这需要制备呋喃苯并二恶英并进一步使环加成的双环加合物脱水。
更新日期:1996-06-01
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