Issue 69, 2012
From the journal:

Chemical Communications

Hydrogenolysis–hydrogenation of aryl ethers: selectivity pattern†

Bhupesh S. Samant*a  and  George W. Kabalkabc  

* Corresponding authors

a Division of Pharmaceutical chemistry, Faculty of Pharmacy, Rhodes University, Grahamstown-6140, South Africa
E-mail: B.Samant@ru.ac.za
Fax: +27 466361205
Tel: +27 466038395

b University of Tennessee, Departments of Chemistry and Radiology, 1420 Circle Drive, Knoxville, USA

c UT Medical Hospital, Biomedical Imaging Center, Knoxville, USA

Abstract

The selectivity pattern of nickel-catalyzed hydrogenolysis–hydrogenation of aryl ethers has been studied in the micellar media. The micellar conditions selectively formed arenes and alcohols with enhanced yields.

Graphical abstract: Hydrogenolysis–hydrogenation of aryl ethers: selectivity pattern

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Article information

DOI
https://doi.org/10.1039/C2CC34454H
Article type
Communication
Submitted
21 Jun 2012
Accepted
04 Jul 2012
First published
04 Jul 2012

Chem. Commun., 2012,48, 8658-8660

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Hydrogenolysis–hydrogenation of aryl ethers: selectivity pattern

B. S. Samant and G. W. Kabalka, Chem. Commun., 2012, 48, 8658 DOI: 10.1039/C2CC34454H

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