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Regioselective Wacker-Type Oxidation of Internal Olefins in tBuOH Using Oxygen as the Sole Oxidant and tBuONO as the Organic Redox Cocatalyst.

Qing HuangYa-Wei LiXiao-Shan NingGuo-Qing JiangXiao-Wei ZhangJian-Ping QuYan-Biao Kang
Published in: Organic letters (2020)
A regioselective Wacker-Tsuji oxidation of internal olefins in tBuOH has been developed using oxygen as the terminal oxidant and tert-butyl nitrite as the simple organic redox cocatalyst without the involvement of hazardous cocatalysts or harsh reaction conditions. A series of internal olefins bearing various functional groups can be oxidized to the corresponding substituted ketones in generally good yields with high regioselectivities.
Keyphrases
  • electron transfer
  • hydrogen peroxide
  • nitric oxide
  • water soluble
  • molecular docking