A convenient synthesis of polysubstituted phenylphenols from substituted anilines

2' and 4'-Substituted arylfurans react with DMAD in the presence of Lewis acid to afford Diels-Alder adducts with good yields; a subsequent spontaneous or an acid-induced beta-elimination leads to polysubstituted phenylphenols.

Saved in:
Bibliographic Details
Published inSynthesis (Stuttgart) no. 6; pp. 631 - 634
Main Authors Maggiani, A, Tubul, A, Brun, P
Format Journal Article
LanguageEnglish
Published STUTTGART Thieme Medical Publishers 01.06.1997
Subjects
Chemistry
Chemistry, Organic
Physical Sciences
Science & Technology
FURAN
DIELS-ALDER REACTION
Online AccessGet more information

Cover

More Information
Summary:2' and 4'-Substituted arylfurans react with DMAD in the presence of Lewis acid to afford Diels-Alder adducts with good yields; a subsequent spontaneous or an acid-induced beta-elimination leads to polysubstituted phenylphenols.
ISSN:0039-7881
DOI:10.1055/s-1997-1403