Beckmann rearrangement
id:
beckmann-rearrangement-208-1335713
title:
Beckmann rearrangement
text:
The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is a rearrangement of an oxime functional group to substituted amides. The rearrangement has also been successfully performed on haloimines and nitrones. Cyclic oximes and haloimines yield lactams. The Beckmann rearrangement is often catalyzed by acid; however, other reagents have been known to promote the rearrangement. These include tosyl chloride, thionyl chloride, phosphorus pentachloride, phosphorus
brand slug:
wiki
category slug:
encyclopedia
description:
Chemical rearrangement
original url:
https://en.wikipedia.org/wiki/Beckmann_rearrangement
date created:
2003-06-23T11:42:15Z
date modified:
2024-09-11T05:50:17Z
main entity:
{"identifier":"Q813746","url":"https://www.wikidata.org/entity/Q813746"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/e/eb/BeckmannRearrangement3.svg","width":391,"height":145}
fields total:
13
integrity:
16