Dienone–phenol rearrangement
id:
dienone-phenol-rearrangement-260-9642475
title:
Dienone–phenol rearrangement
text:
The dienone–phenol rearrangement is a reaction in organic chemistry first reported in 1921 by Karl von Auwers and Karl Ziegler. A common example of dienone–phenol rearrangement is 4,4-disubstituted cyclohexadienone converting into a stable 3,4-disubstituted phenol in presence of acid. A similar rearrangement is possible with a 2,2-disubstituted cyclohexadienone to its corresponding disubstituted phenol. Usually this type of rearrangement is spontaneous unless a dichloromethyl group is present at
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wiki
category slug:
encyclopedia
description:
original url:
https://en.wikipedia.org/wiki/Dienone%E2%80%93phenol_rearrangement
date created:
date modified:
2022-05-28T22:30:07Z
main entity:
{"identifier":"Q11309460","url":"https://www.wikidata.org/entity/Q11309460"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/4/4a/Dienone-phenol_rearrangement_scheme.svg","width":617,"height":336}
fields total:
13
integrity:
14