A Highly Selective Catalytic Method for the Oxidative Functionalization of C−H Bonds
Journal of the American Chemical Society2004Vol. 126(8), pp. 2300–2301
Citations Over TimeTop 1% of 2004 papers
Abstract
This communication describes a new and highly practical Pd(II)-catalyzed method for the regio- and chemoselective oxidative functionalization of arenes and alkanes. Carbon-hydrogen bonds of substrates that contain a variety of directing groups (e.g., pyridine, azobenzene, pyrazole, and imine derivatives) are selectively transformed into esters, ethers, and aryl-halides under mild conditions. The scope of this reaction in terms of substrate, directing group, and oxidant is described, and a preliminary catalytic cycle is proposed.
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