One-pot tandem approach to spirocyclic oxindoles featuring adjacent spiro-stereocenters

Angew Chem Int Ed Engl. 2013 Dec 16;52(51):13735-9. doi: 10.1002/anie.201307250. Epub 2013 Nov 7.

Abstract

All in a sequence: An organocatalyzed Morita-Baylis-Hillman (MBH)/bromination/[3+2] annulation sequence for highly stereoselective syntheses of bis(spirooxindole)s featuring adjacent spiro-stereocenters is described. The key step is an unprecedented catalytic asymmetric [3+2] annulation of isatin-derived MBH adducts, containing a tetrasubstituted alkene moiety, with isatins.

Keywords: asymmetric catalysis; heterocycles; organocatalysis; spiro compounds; synthetic methods.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Indoles / chemistry*
  • Molecular Structure
  • Oxindoles
  • Spiro Compounds / chemistry*
  • Stereoisomerism

Substances

  • Indoles
  • Oxindoles
  • Spiro Compounds
  • 2-oxindole