Asymmetric dearomatization of indoles through a Michael/Friedel-Crafts-type cascade to construct polycyclic spiroindolines

Angew Chem Int Ed Engl. 2015 Mar 23;54(13):4032-5. doi: 10.1002/anie.201410814. Epub 2015 Feb 3.

Abstract

A highly efficient asymmetric dearomatization of indoles was realized through a cascade reaction between 2-isocyanoethylindole and alkylidene malonates catalyzed by a chiral N,N'-dioxide/Mg(II) catalyst. Fused polycyclic indolines containing three stereocenters were afforded in good yields with excellent diastereo- and enantioselectivities through a Michael/Friedel-Crafts/Mannich cascade. When 2-substituted 2-isocyanoethylindoles were used, spiroindoline derivatives were obtained through a Michael/Friedel-Crafts reaction.

Keywords: aromaticity; asymmetric catalysis; cascade reactions; heterocycles; magnesium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Indicators and Reagents
  • Indoles / chemical synthesis*
  • Kinetics
  • Malonates / chemistry
  • Mannich Bases
  • Molecular Conformation
  • Polycyclic Compounds / chemical synthesis*
  • Stereoisomerism
  • X-Ray Diffraction

Substances

  • Indicators and Reagents
  • Indoles
  • Malonates
  • Mannich Bases
  • Polycyclic Compounds
  • indoline