Highly effective vinylogous Mukaiyama-Michael reaction catalyzed by silyl methide species generated from 1,1,3,3-tetrakis(trifluoromethanesulfonyl)propane

J Org Chem. 2010 Feb 19;75(4):1259-65. doi: 10.1021/jo902641g.

Abstract

Silyl methide species in situ generated from 1,1,3,3-tetrakis(trifluoromethanesulfonyl)propane (Tf(2)CHCH(2)CHTf(2)) performed as an excellent acid catalyst for the vinylogous Mukaiyama-Michael reaction of alpha,beta-unsaturated ketones with 2-silyloxyfurans. Notably, the required loading of Tf(2)CHCH(2)CHTf(2) to obtain the 1,4-adducts in reasonable yield was significantly low (from 0.05 to 1.0 mol %). This carbon acid-mediated VMM reaction provides a powerful synthetic methodology to construct highly substituted gamma-butenolide structure.

MeSH terms

  • Catalysis
  • Furans / chemistry*
  • Hydrocarbons, Fluorinated / chemistry*
  • Ketones / chemistry
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Molecular Structure
  • Organosilicon Compounds / chemistry*
  • Propane / analogs & derivatives*
  • Propane / chemistry
  • Stereoisomerism

Substances

  • 1,1,3,3-tetrakis(trifluoromethanesulfonyl)propane
  • Furans
  • Hydrocarbons, Fluorinated
  • Ketones
  • Organosilicon Compounds
  • Propane