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Palladium-Catalyzed Cross-Coupling Reaction of (E)-1-Alkenyl-1,3,2-benzo-dioxaboroles with Allylic Phenoxides. A Simple Route 1,4-Alkadienes from Alkynes via Hydroboration$^\dag$

  • Sasaya Fumihito (Department of Applied Chemistry, Faculty of Engineering) ;
  • Norio Miyaura (Department of Applied Chemistry, Faculty of Engineering) ;
  • Akira Suzuki (Department of Applied Chemistry, Faculty of Engineering)
  • Published : 1987.08.20

Abstract

The reaction of (E)-1-alkenyl-1,3,2-benzodioxaboroles with a variety of allylic phenoxides in the presence of a catalytic amount of Pd$(PPh_3)_4$ is described. The reaction affords a general and simple procedure for the preparation of 1,4-alkadienes from alkynes via hydroboration.

Keywords

References

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  3. Synthesis of Trifluoromethyl Ketones by Palladium-Catalyzed Cross-Coupling Reaction of Phenyl Trifluoroacetate with Organoboron Compounds vol.74, pp.2, 2001, https://doi.org/10.1246/bcsj.74.371
  4. Palladium-Catalyzed Direct Conversion of Carboxylic Acids into Ketones with Organoboronic Acids Promoted by Anhydride Activators vol.75, pp.6, 1987, https://doi.org/10.1246/bcsj.75.1333
  5. Synthesis of Unsymmetrical Ketones by Palladium-Catalyzed Cross-Coupling Reaction of Carboxylic Anhydrides with Organoboron Compounds vol.75, pp.1, 1987, https://doi.org/10.1246/bcsj.75.137
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