Versatile Alkylation of (Hetero)Aryl Iodides with Ketones via β-C(sp3)-H Activation

J Am Chem Soc. 2017 Nov 15;139(45):16080-16083. doi: 10.1021/jacs.7b09761. Epub 2017 Nov 3.

Abstract

We report Pd(II)-catalyzed β-C(sp3)-H (hetero)arylation of a variety of ketones using a commercially available 2,2-dimethyl aminooxyacetic acid auxiliary. Facile installation and removal of the auxiliary as well as its superior scope for both ketones and (hetero)aryl iodides overcome the significant limitations of the previously reported β-C(sp3)-H arylation of ketones. The ready availability of ketones renders this reaction a broadly useful method for alkyl-(hetero)aryl coupling involving both primary and secondary alkyls.

Publication types

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

MeSH terms

  • Alkylation
  • Aminooxyacetic Acid / chemical synthesis
  • Aminooxyacetic Acid / chemistry
  • Catalysis
  • Hydrocarbons, Aromatic / chemical synthesis
  • Hydrocarbons, Aromatic / chemistry*
  • Iodides / chemical synthesis
  • Iodides / chemistry*
  • Ketones / chemical synthesis
  • Ketones / chemistry*
  • Palladium / chemistry*

Substances

  • Hydrocarbons, Aromatic
  • Iodides
  • Ketones
  • Aminooxyacetic Acid
  • Palladium