articleJournal of the American Chemical SocietyFeb 3, 2004Closed access

A Highly Selective Catalytic Method for the Oxidative Functionalization of C−H Bonds

University of Michigan–Ann Arbor

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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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1,050
total citations
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16.53
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100%
References
23
Citations per year

Authors

3

Topics & keywords

Keywords
  • Chemistry
  • Surface modification
  • Catalysis
  • Aryl
  • Imine
  • Catalytic cycle
  • Combinatorial chemistry
  • Substrate (aquarium)
UN Sustainable Development Goals
  • Clean water and sanitation
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