DIELS-ALDER REACTIONS OF FURO[3,4-B]1,4-BENZODIOXINS - AN EFFICIENT APPROACH TO SUBSTITUTED DIBENZO[B,E][1,4]DIOXINS

Authors
RUIZ N BUON C PUJOL MD GUILLAUMET G COUDERT G
Citation
N. Ruiz et al., DIELS-ALDER REACTIONS OF FURO[3,4-B]1,4-BENZODIOXINS - AN EFFICIENT APPROACH TO SUBSTITUTED DIBENZO[B,E][1,4]DIOXINS, Synthetic communications, 26(11), 1996, pp. 2057-2066
Citations number
24
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthetic communications → ACNP
ISSN journal
00397911
Volume
26
Issue
11
Year of publication
1996
Pages
2057 - 2066
Database
ISI
SICI code
0039-7911(1996)26:11<2057:DROF-A>2.0.ZU;2-4
Abstract
In view of their potential biological properties, different substitute d dibenzo [b,e][1,4] dioxins have been synthesized using Diels-Alder r eactions. This required the preparation of furobenzodioxins and furthe r dehydration of the bicyclo-adducts of the cycloaddition.