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

Kiyofumi Inamoto; Kanako Nozawa; Misato Yonemoto; Yoshinori Kondo

doi:10.1039/c1cc14974a

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

Chem Commun (Camb). 2011 Nov 14;47(42):11775-7. doi: 10.1039/c1cc14974a. Epub 2011 Sep 30.

Authors

Kiyofumi Inamoto¹, Kanako Nozawa, Misato Yonemoto, Yoshinori Kondo

Affiliation

¹ Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3, Aoba, Aramaki, Sendai 980-8578, Japan. inamoto@mail.pharm.tohoku.ac.jp

PMID: 21959336
DOI: 10.1039/c1cc14974a

Abstract

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

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Boronic Acids / chemistry*
Catalysis
Copper / chemistry*
Hydroxylation
Magnetic Resonance Spectroscopy
Micelles*
Phenols / chemistry*

Substances

Boronic Acids
Micelles
Phenols
Copper