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

被引：16
|
作者：
Ruiz, N
Buon, C
Pujol, MD
Guillaumet, G
Coudert, G
机构：
[1] UNIV ORLEANS,CHIM BIOORGAN & ANALYT LAB,CNRS,URA 499,F-45067 ORLEANS 2,FRANCE
[2] UNIV BARCELONA,FAC FARM,QUIM FARMACEUT LAB,E-08028 BARCELONA,SPAIN
来源：
SYNTHETIC COMMUNICATIONS | 1996年 / 26卷 / 11期
关键词：
D O I：
10.1080/00397919608003564
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
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.
引用
收藏
页码：2057 / 2066
页数：10
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