Communication
C
X (X=Br, I) Bond-Tolerant Aerobic Oxidative Cross- Coupling: A Strategy to Selectively Construct β-Aryl Ketones and Aldehydes
Article first published online: 9 FEB 2012
DOI: 10.1002/adsc.201100782
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Chen, M., Wang, J., Chai, Z., You, C. and Lei, A. (2012), C
X (X=Br, I) Bond-Tolerant Aerobic Oxidative Cross- Coupling: A Strategy to Selectively Construct β-Aryl Ketones and Aldehydes. Adv. Synth. Catal., 354: 341–346. doi: 10.1002/adsc.201100782
Publication History
- Issue published online: 17 FEB 2012
- Article first published online: 9 FEB 2012
- Manuscript Received: 8 OCT 2011
Funded by
- National Natural Science Foundation of China. Grant Number: 20702040, 20832003, 20972118
Keywords:
- copper;
- cross-coupling;
- oxygen;
- palladium;
- selectivity
Abstract
Using moelcular oxygen as the terminal oxidant, various aryl halide-containing β-aryl ketones and aldehydes can be synthesized directly from readily available allyic alcohols and boronic acids via palladium-catalyzed oxidative cross-coupling reactions. The dual roles of copper, including electron-carrier and Lewis acid functions, are supposed to be critical for the high reactivity and selectivity of this aerobic oxidative coupling transformation.

1615-4169/asset/2258_left.gif?v=1&s=480b85eb3acd0e8f47639c75e9ec7a59d53cd074)
