Stevens rearrangement
id:
stevens-rearrangement-323-15719410
title:
Stevens rearrangement
text:
The Stevens rearrangement in organic chemistry is an organic reaction converting quaternary ammonium salts and sulfonium salts to the corresponding amines or sulfides in presence of a strong base in a 1,2-rearrangement. The reactants can be obtained by alkylation of the corresponding amines and sulfides. The substituent R next the amine methylene bridge is an electron-withdrawing group. The original 1928 publication by Thomas S. Stevens concerned the reaction of 1-phenyl-2-(N,N-dimethylamino)eth
brand slug:
wiki
category slug:
encyclopedia
description:
original url:
https://en.wikipedia.org/wiki/Stevens_rearrangement
date created:
date modified:
2023-04-06T02:43:18Z
main entity:
{"identifier":"Q906103","url":"https://www.wikidata.org/entity/Q906103"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/3/3c/Stevens_rearrangement_overview.svg","width":516,"height":318}
fields total:
13
integrity:
14