Issue 35, 2014

Direct intermolecular C–H arylation of unactivated arenes with aryl bromides catalysed by 2-pyridyl carbinol

Abstract

Direct intermolecular C–H arylation employing aryl bromide as the arene source has been developed. This process proceeds via a simple transition-metal-free pathway. With the aid of inexpensive and commercially available 2-pyridyl carbinol and potassium tert-butoxide, various unactivated arene C–H bonds can be directly arylated by aryl bromides through homolytic aromatic substitution.

Graphical abstract: Direct intermolecular C–H arylation of unactivated arenes with aryl bromides catalysed by 2-pyridyl carbinol

Supplementary files

Article information

Article type
Communication
Submitted
12 Jun 2014
Accepted
23 Jul 2014
First published
23 Jul 2014

Org. Biomol. Chem., 2014,12, 6820-6823

Author version available

Direct intermolecular C–H arylation of unactivated arenes with aryl bromides catalysed by 2-pyridyl carbinol

Y. Wu, P. Y. Choy and F. Y. Kwong, Org. Biomol. Chem., 2014, 12, 6820 DOI: 10.1039/C4OB01211A

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