Issue 4, 2005
From the journal:

Organic & Biomolecular Chemistry

Methoxy-substituted centrohexaindanes through the fenestrane route†

Jörg Tellenbröker,a   Dieter Barth,a   Beate Neumann,a   Hans-Georg Stammlera  and  Dietmar Kuck*a  

* Corresponding authors

a Fakultät für Chemie, Universität Bielefeld, Universitätsstraße 25, Bielefeld, Germany
E-mail: dietmar.kuck@uni-bielefeld.de
Fax: (+49) 521 106-6417
Tel: (+49) 521 106-2060

Abstract

Tetrahydroxyfenestrindane undergoes HPF6-catalyzed condensation with anisole, 2-methylanisole and the three dimethoxybenzenes to furnish several centrohexaindanes bearing oxyfunctionalization at the opposite ends of one of the three [2,2′]-spirobiindane axes.

Graphical abstract: Methoxy-substituted centrohexaindanes through the fenestrane route

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Article information

DOI
https://doi.org/10.1039/B417837H
Article type
Communication
Submitted
24 Nov 2004
Accepted
01 Dec 2004
First published
05 Jan 2005

Org. Biomol. Chem., 2005,3, 570-571

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Methoxy-substituted centrohexaindanes through the fenestrane route

J. Tellenbröker, D. Barth, B. Neumann, H. Stammler and D. Kuck, Org. Biomol. Chem., 2005, 3, 570 DOI: 10.1039/B417837H

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