Published in

Royal Society of Chemistry, New Journal of Chemistry, 3(36), p. 570

DOI: 10.1039/c2nj21033a

Links

Tools

Export citation

Search in Google Scholar

Tetraazaarenes by the ceramidonine approach

Journal article published in 2012 by Parantap Sarkar, Ie-Rang Jeon, Fabien Durola ORCID, Harald Bock
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

The synthesis of extended heteroarenes via the acid-promoted dehydrocyclisation of arylamino-anthraquinones is examined as an approach to highly conjugated electron-acceptor materials and eventually to heterographene nanoribbons. Whilst the latter perspective is found to remain challenging, the former is exemplified by the synthesis of extended tetraazaheterocycles bearing solubilising alkyl substituents. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2012.