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Accessing para -Alkylphenols via Iridium-Catalyzed Site-Specific Deoxygenation of Alcohols.

Jing WangTingting WangHongguang DuNing ChenJiaxi XuZhanhui Yang
Published in: The Journal of organic chemistry (2023)
An iridium-catalyzed and phenol-directed deoxygenation of benzylic alcohols comes as an alternative access to 4-alkylphenols, featuring low catalyst loading ( S / C up to 20,000, TOF up to 12,400 h -1 ), high functionality compatibility, and excellent site-selectivity. The applications in late-stage modification of steroids and gram-scale total synthesis of a Gastrodia elata extract are highlighted. Mechanistically, the intermediacy of quinone methide controls the site-selectivity, and the formation of iridium hydride serves as the rate-limiting step.
Keyphrases
  • room temperature
  • mass spectrometry
  • ms ms
  • ionic liquid
  • gram negative
  • oxidative stress
  • highly efficient
  • multidrug resistant
  • metal organic framework