Isoindole
From Wikipedia, the free encyclopedia
Isoindole in heterocyclic chemistry is a benzo fused pyrrole [1]. The compound is an isomer of indole and its reduced form is an isoindoline.
In solution the non-aromatic tautomer is predominant:
and therefore the compound resembles a pyrrole more than a simple imine. Isoindoles are building blocks for phthalocyanines which are relevant as dyes
[edit] Isoindole-1,3-diones
The commercially important phthalimide is an isoindole-1,3-dione with two carbonyl groups attached to the heterocyclic ring. Thalidomide is an infamous drug based on this framework.
[edit] See also
[edit] References
- ^ Heterocyclic chemistry T.L. Gilchrist ISBN 0852014220