Ligand-controlled regiodivergent palladium-catalyzed decarboxylative allylation reaction to access α,α-difluoroketones

Angew Chem Int Ed Engl. 2015 Feb 16;54(8):2361-5. doi: 10.1002/anie.201410039. Epub 2015 Jan 7.

Abstract

α,α-Difluoroketones possess unique physicochemical properties that are useful for developing therapeutics and probes for chemical biology. To access the α-allyl-α,α-difluoroketone substructure, complementary palladium-catalyzed decarboxylative allylation reactions were developed to provide linear and branched α-allyl-α,α-difluoroketones. For these orthogonal processes, the fluorination pattern of the substrate enabled the ligands to dictate the regioselectivity of the transformations.

Keywords: allylation; fluorine; palladium; phosphine ligands; regioselectivity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Allyl Compounds / chemistry
  • Catalysis
  • Halogenation
  • Ketones / chemistry*
  • Ligands*
  • Palladium / chemistry*
  • Phosphines / chemistry
  • Stereoisomerism

Substances

  • Allyl Compounds
  • Ketones
  • Ligands
  • Phosphines
  • Palladium