Stereoselective synthesis of acetoacetate-derived enol triflates

Org Lett. 2008 Jul 3;10(13):2901-4. doi: 10.1021/ol8010002. Epub 2008 Jun 10.

Abstract

A highly stereoselective method for preparing ( Z)- and ( E)-enol triflates derived from substituted acetoacetate derivatives is described. The salient feature of this methodology is the use of Schotten-Baumann-type conditions to control enolate geometry using either aqueous LiOH ( Z-selective) or aqueous (Me)(4)NOH ( E-selective) in combination with triflic anhydride to provide a practical and predictable approach to these valuable substrates.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetoacetates / chemistry*
  • Mesylates / chemical synthesis*
  • Mesylates / chemistry
  • Molecular Structure
  • Stereoisomerism

Substances

  • Acetoacetates
  • Mesylates
  • acetoacetic acid