Skattebøl rearrangement
id:
skatteb-l-rearrangement-299-9140626
title:
Skattebøl rearrangement
text:
The Skattebøl rearrangement is an organic reaction for converting a geminal dihalo cyclopropane to an allene using an organolithium base. This rearrangement reaction is named after its discoverer, Lars Skattebøl, Professor emeritus at the University of Oslo. It proceeds through a carbene reaction intermediate: When the cyclopropane ring is fitted with a 2-vinyl group, a cyclopentadiene is formed through a so-called foiled carbene intermediate. This process is more generally known as a vinylcyclo
brand slug:
wiki
category slug:
encyclopedia
description:
Organic reaction
original url:
https://en.wikipedia.org/wiki/Skatteb%C3%B8l_rearrangement
date created:
date modified:
2023-03-05T14:45:00Z
main entity:
{"identifier":"Q899193","url":"https://www.wikidata.org/entity/Q899193"}
image:
fields total:
13
integrity:
14