Organocatalytic tandem Morita-Baylis-Hillman-Michael reaction for asymmetric synthesis of a drug-like oxa-spirocyclic indanone scaffold

Chem Commun (Camb). 2013 Oct 7;49(77):8692-4. doi: 10.1039/c3cc44004d.

Abstract

A novel multicatalytic MBH-Michael tandem reaction has been developed for the asymmetric assembly of ninhydrin, nitroolefins and aldehydes into a structurally complex oxa-spirocyclic indanone backbone. Successive iodocyclization allowed us to convert these multifunctional allylic products into fused chiral natural product mimics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry
  • Alkenes / chemistry
  • Catalysis
  • Cyclization
  • Indans / chemical synthesis*
  • Indans / chemistry
  • Ninhydrin / chemistry
  • Stereoisomerism

Substances

  • Aldehydes
  • Alkenes
  • Indans
  • indacrinone
  • Ninhydrin