Skip to the main content

Review article

https://doi.org/10.15255/KUI.2013.004

Derivatives of Isoindoline, Synthesis and Biological Activity.
I. Natural and Synthetic Derivatives of Isoindoline

I. Sović ; Department of Organic Chemistry Faculty of Chemical Engineering and Technology University of Zagreb, Zagreb Croatia
G. Karminski-Zamola ; Department of Organic Chemistry Faculty of Chemical Engineering and Technology University of Zagreb, Zagreb Croatia


Full text: croatian pdf 1.017 Kb

versions

page 173-182

downloads: 890

cite


Abstract

Derivatives of isoindolines are a group of nitrogen heterocyclic compounds that are less represented in scientific literature than other heterocyclic compounds containing the nitrogen atom. Natural derivatives of isoindolines were first isolated in the early 1960's and showed various interesting biological activity, e.g. staurosporine indicating antimicrobial, hypotensive, and cytotoxic activity, and acts as thrombocytes aggregation inhibitor and protein kinase inhibitor. Also, there are reports of their application in herbicide and dye industries. Due to these findings, isoindolines received much attention from synthetic organic chemists, and thus new synthetic methods were developed. Most of the methods include phthalaldehyde and corresponding aliphatic and aromatic amines as starting material. Products of these reactions are highly dependent on the reaction conditions, and differently substituted isoindolines are isolated. Synthetic methods starting from other compounds include phthalonitrile, phthalanhydride and phthalaldehyde acid as well as multicomponent reactions. They are also applied as ligands in coordination chemistry, which enables the modelling of
three-dimensional structures with desirable areal properties.

Keywords

Heterocyclic compounds; isoindoline derivatives; natural isoindolines; synthetic isoindolines

Hrčak ID:

120640

URI

https://hrcak.srce.hr/120640

Publication date:

6.5.2014.

Article data in other languages: croatian

Visits: 1.930 *