Fukuyama indole synthesis
id:
fukuyama-indole-synthesis-323-12307065
title:
Fukuyama indole synthesis
text:
The Fukuyama indole synthesis is a versatile tin mediated chemical reaction that results in the formation of 2,3-disubstituted indoles. A practical one-pot reaction that can be useful for the creation of disubstituted indoles. Most commonly tributyltin hydride is utilized as the reducing agent, with azobisisobutyronitrile (AIBN) as a radical initiator. Triethylborane can also be used as a radical initiator. The reaction can begin with either an ortho-isocyanostyrene or a 2-alkenylthioanilide der
brand slug:
wiki
category slug:
encyclopedia
description:
Chemical organic reaction
original url:
https://en.wikipedia.org/wiki/Fukuyama_indole_synthesis
date created:
date modified:
2024-02-24T09:50:23Z
main entity:
{"identifier":"Q3118805","url":"https://www.wikidata.org/entity/Q3118805"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/f/f9/Fukuyama_Indole_Synthesis_Showing_Both_Potential_Starting_Reagents.png","width":718,"height":411}
fields total:
13
integrity:
15