| Literature DB >> 28177235 |
Qi-Liang Yang1,2, Yi-Qian Li1, Cong Ma1, Ping Fang1, Xiu-Jie Zhang1, Tian-Sheng Mei1.
Abstract
Palladium-catalyzed C-H activation/C-O bond-forming reactions have emerged as attractive tools for organic synthesis. Typically, these reactions require strong chemical oxidants, which convert organopalladium(II) intermediates into the PdIII or PdIV oxidation state to promote otherwise challenging C-O reductive elimination. However, previously reported oxidants possess significant disadvantages, including poor atom economy, high cost, and the formation of undesired byproducts. To overcome these issues, we report an electrochemical strategy that takes advantage of anodic oxidation of PdII to induce selective C-O reductive elimination with a variety of oxyanion coupling partners.Entities:
Year: 2017 PMID: 28177235 DOI: 10.1021/jacs.7b01232
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419