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Palladium(0)-Catalyzed Dearomative [3 + 2] Cycloaddition of 3-Nitroindoles with Vinylcyclopropanes: An Entry to Stereodefined 2,3-Fused Cyclopentannulated Indoline Derivatives.

Maxime LaugeoisJohanne LingCharlène FérardVéronique MicheletVirginie Ratovelomanana-VidalMaxime R Vitale
Published in: Organic letters (2017)
The palladium(0)-catalyzed diastereoselective dearomative cyclopentannulation of 3-nitroindoles with vinylcyclopropanes is described. This straightforward and highly atom-economical method leads to a wide range of functionalized indolines in good yields and diastereoselectivities and represents an unprecedented entry toward the valuable 2,3-fused cyclopentannulated indoline scaffold.
Keyphrases
  • molecular dynamics
  • quantum dots
  • tissue engineering
  • molecularly imprinted
  • mass spectrometry