Issue 20, 2010
From the journal:

Chemical Communications

Arylsilaneoxidation—new routes to hydroxylated aromatics†

Sonia Bracegirdlea  and  Edward A. Anderson*a  

* Corresponding authors

a Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, UK
E-mail: edward.anderson@chem.ox.ac.uk
Fax: +44 (0)1865 285002
Tel: +44 (0)1865 285000

Abstract

An efficient route to hydroxylated aromatics has been developed, via the oxidation of aryl organosilanes under functional group-tolerant and relatively mild conditions, using sub-stoichiometric amounts of fluoride promoters.

Graphical abstract: Arylsilane oxidation—new routes to hydroxylated aromatics

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Article information

DOI
https://doi.org/10.1039/B924135C
Article type
Communication
Submitted
18 Nov 2009
Accepted
21 Dec 2009
First published
13 Jan 2010

Chem. Commun., 2010,46, 3454-3456

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Arylsilane oxidation—new routes to hydroxylated aromatics

S. Bracegirdle and E. A. Anderson, Chem. Commun., 2010, 46, 3454 DOI: 10.1039/B924135C

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