Enantioselective direct vinylogous Michael addition of functionalized furanones to nitroalkenes catalyzed by an axially chiral guanidine base

Org Lett. 2011 Apr 15;13(8):2026-9. doi: 10.1021/ol200415u. Epub 2011 Mar 18.

Abstract

The highly syn-diastereo- and enantioselective direct vinylogous Michael addition of α-thio substituted furanones with conjugate nitroalkenes was demonstrated using an axially chiral guanidine base catalyst. The method provides facile access to enantioenriched α,γ-functionalized butenolides that can be further manipulated, thereby rendering them useful synthetic intermediates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Catalysis
  • Furans / chemistry*
  • Guanidine / chemistry*
  • Molecular Structure
  • Nitro Compounds / chemistry*
  • Stereoisomerism
  • Vinyl Compounds / chemistry*

Substances

  • Alkenes
  • Furans
  • Nitro Compounds
  • Vinyl Compounds
  • Guanidine
  • furan