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Palladium/TY-Phos-Catalyzed Asymmetric Heck/Tsuji-Trost Reaction of o -Bromophenols with 1,3-Dienes.

Youshao TuBing XuQian WangHonglin DongZhan-Ming ZhangJunliang Zhang
Published in: Journal of the American Chemical Society (2023)
2,3-Dihydrobenzofurans are crucial building blocks in the synthesis of natural products and pharmaceutical molecules. However, their asymmetric synthesis has been a long-standing formidable challenge so far. In this work, we developed a highly enantioselective Pd/TY-Phos-catalyzed Heck/Tsuji-Trost reaction of o -bromophenols with various 1,3-dienes, allowing expedient access to chiral substituted 2,3-dihydrobenzofurans. This reaction features excellent regio- and enantiocontrol, high functional group tolerance, and easy scalability. More importantly, the demonstration of this method as a highly valuable tool for the construction of optically pure natural products ( R )-tremetone and fomannoxin is highlighted.
Keyphrases
  • room temperature
  • molecular docking
  • solid state
  • mass spectrometry
  • capillary electrophoresis