Issue 42, 2011
From the journal:

Chemical Communications

Micellar system in copper-catalysed hydroxylation of arylboronic acids: facile access to phenols†

Kiyofumi Inamoto,*a   Kanako Nozawa,a   Misato Yonemotoa  and  Yoshinori Kondo*a  

* Corresponding authors

a Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3, Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan
E-mail: inamoto@mail.pharm.tohoku.ac.jp, ykondo@mail.pharm.tohoku.ac.jp
Fax: +81-22-795-3921
Tel: +81-22-795-6804

Abstract

Copper-catalysed oxidative hydroxylation of arylboronic acids was accomplished in water containing an amphiphilic surfactant, providing facile access to phenol derivatives.

Graphical abstract: Micellar system in copper-catalysed hydroxylation of arylboronic acids: facile access to phenols

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Article information

DOI
https://doi.org/10.1039/C1CC14974A
Article type
Communication
Submitted
11 Aug 2011
Accepted
21 Sep 2011
First published
30 Sep 2011

Chem. Commun., 2011,47, 11775-11777

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Micellar system in copper-catalysed hydroxylation of arylboronic acids: facile access to phenols

K. Inamoto, K. Nozawa, M. Yonemoto and Y. Kondo, Chem. Commun., 2011, 47, 11775 DOI: 10.1039/C1CC14974A

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