Fe-catalyzed Decarbonylative Alkylative Spirocyclization of N-Arylcinnamamides: Access to Alkylated 1-Azaspirocyclohexadienones

Molecules. 2020 Jan 21;25(3):432. doi: 10.3390/molecules25030432.

Abstract

For the convenient introduction of simple linear/branched alkyl groups into biologically important azaspirocyclohexadienones, a practical Fe-catalyzed decarbonylative cascade spiro-cyclization of N-aryl cinnamamides with aliphatic aldehydes to provide alkylated 1-azaspiro-cyclohexadienones was developed. Aliphatic aldehydes were oxidative decarbonylated into primary, secondary and tertiary alkyl radicals conveniently and allows for the subsequent cascade construction of dual C(sp3)-C(sp3) and C=O bonds via radical addition, spirocyclization and oxidation sequence.

Keywords: aldehyde; alkylation; cinnamamide; decarbonylation; spirocyclization.

MeSH terms

  • Aldehydes / chemistry
  • Alkylating Agents / chemistry*
  • Alkylation
  • Aza Compounds / chemistry*
  • Catalysis
  • Cinnamates / chemistry*
  • Cyclization
  • Cyclohexenes / chemistry*
  • Iron / chemistry*
  • Spiro Compounds / chemistry*

Substances

  • Aldehydes
  • Alkylating Agents
  • Aza Compounds
  • Cinnamates
  • Cyclohexenes
  • Spiro Compounds
  • cyclohexadienone
  • Iron
  • cinnamamide