Zincke–Suhl reaction
id:
zincke-suhl-reaction-238-18174271
title:
Zincke–Suhl reaction
text:
The Zincke–Suhl reaction is a special case of a Friedel-Crafts alkylation and was first described by Theodor Zincke and Suhl in 1906. Unlike the traditional Friedel-Crafts reaction, the reduction of the phenyl ring leads to a higher energy final product that can be used as starting material in the dienol–benzene rearrangement, among other reactions. The classic example of this reaction is the conversion of p-cresol to a cyclohexadienone. Melvin Newman, a scientist from the U.S. intensively studi
brand slug:
wiki
category slug:
encyclopedia
description:
original url:
https://en.wikipedia.org/wiki/Zincke%E2%80%93Suhl_reaction
date created:
date modified:
2023-02-17T16:03:06Z
main entity:
{"identifier":"Q2273953","url":"https://www.wikidata.org/entity/Q2273953"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/a/a8/Zinckesuhl.svg","width":772,"height":357}
fields total:
13
integrity:
14