4.7 Article

C?X (X=Br, I) Bond-Tolerant Aerobic Oxidative Cross- Coupling: A Strategy to Selectively Construct ß-Aryl Ketones and Aldehydes

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 354, Issue 2-3, Pages 341-346

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201100782

Keywords

copper; cross-coupling; oxygen; palladium; selectivity

Funding

  1. National Natural Science Foundation of China [20702040, 20832003, 20972118]

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Using moelcular oxygen as the terminal oxidant, various aryl halide-containing beta-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.

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