Issue 17, 2010
From the journal:

Organic & Biomolecular Chemistry

New class of highly stable nonaromatic tautomers†

Claire Seillan,a   Philippe Marsala  and  Olivier Siri*a  

* Corresponding authors

a Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), UPR 3118 CNRS Aix-Marseille Université, Campus de Luminy, case 913 F-13288, Marseille cedex 09, France
E-mail: siri@univmed.fr
Fax: +33-491-829-580
Tel: +33-617-248-134

Abstract

A new and efficient one-pot synthesis of highly stable bridged-bisphenazine-type molecules with loss of their aromaticity in the ground state in favor of a quinoid-type structure is described (either in solution or in solid-state).

Graphical abstract: New class of highly stable nonaromatic tautomers

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Article information

DOI
https://doi.org/10.1039/C003450A
Article type
Paper
Submitted
23 Feb 2010
Accepted
28 May 2010
First published
02 Jul 2010

Org. Biomol. Chem., 2010,8, 3882-3887

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New class of highly stable nonaromatic tautomers

C. Seillan, P. Marsal and O. Siri, Org. Biomol. Chem., 2010, 8, 3882 DOI: 10.1039/C003450A

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