4.8 Article

Nickel-Catalyzed Oxidative Carbonylation of Alkylarenes to Arylacetic Acids

Journal

ORGANIC LETTERS
Volume 24, Issue 43, Pages 7972-7977

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c03121

Keywords

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Funding

  1. National Natural Science Foundation of China
  2. China Postdoctoral Science Foundation
  3. Strate- gic Priority Research Program of the CAS
  4. USTC-Yanchang Petroleum New Energy Joint Research Project
  5. National Key R&D Program of China
  6. [21925111]
  7. [21790333]
  8. [2021M703070]
  9. [XDPB14]
  10. [KD1911040241]
  11. [2021YFA1501003]

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A catalytic system combining NiBr2 and diphenylphosphine oxide was developed for the direct synthesis of valuable arylacetic acids from inexpensive alkylarenes and H2O via oxidative carbonylation. This method is compatible with alkylarenes containing primary and secondary benzylic C-H bonds, and the commonly used drugs ibuprofen and diclofenac can be easily obtained.
A catalytic system combined with NiBr2 and diphenylphosphine oxide that enabled direct access to the valuable arylacetic acids from inexpensive alkylarenes and H2O via oxidative carbonylation was developed. Alkylarenes with primary and secondary benzylic C-H bonds were compatible with this method. Remarkably, the marketed drugs ibuprofen and diclofenac could be easily obtained by this procedure straightforwardly.

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