Superelectrophilic activation in superacid HF/SbF(5) and synthesis of benzofused sultams

Org Lett. 2010 Feb 19;12(4):868-71. doi: 10.1021/ol9029287.

Abstract

The synthesis of benzofused sultams and/or fluorinated sulfonamides, starting from N-allylic sulfonamides, was performed in superacid HF/SbF(5), through superelectrophilic activation. A dramatic effect of superacid composition on the selectivity of the reaction was shown and applied to the synthesis of cyclic 4-aminobenzenesulfonamides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimony / chemistry
  • Catalysis
  • Combinatorial Chemistry Techniques
  • Fluorides / chemistry
  • Hydrocarbons, Fluorinated / chemical synthesis
  • Hydrocarbons, Fluorinated / chemistry
  • Hydrofluoric Acid / chemistry
  • Molecular Structure
  • Sulfanilamide
  • Sulfanilamides / chemical synthesis*
  • Sulfanilamides / chemistry

Substances

  • Hydrocarbons, Fluorinated
  • Sulfanilamides
  • Sulfanilamide
  • antimony pentafluoride
  • Antimony
  • Fluorides
  • Hydrofluoric Acid