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Silylium-Catalyzed Regio- and Stereoselective Carbosilylation of Ynamides with Allylic Trimethylsilanes.

Paz YepesÁngel L Suárez-SobrinoMiguel A RodríguezAlfredo Ballesteros
Published in: Organic letters (2023)
The regio- and stereoselective carbosilylation of tosylynamides with allylic trimethylsilanes takes place under mild conditions in the presence of catalytic TMSNTf 2 or HNTf 2 to give ( Z )-α-allyl-β-trimethylsilylenamides with good yields. Theoretical calculations show the activation of the C-C triple bond of the ynamides by the trimethylsilylium ion and formation of a β-trimethylsilylketenimonium cation. Further transformations of the products demonstrate the synthetic utility of this reaction.
Keyphrases
  • density functional theory
  • molecular dynamics
  • room temperature
  • molecular dynamics simulations
  • ionic liquid
  • monte carlo
  • crystal structure
  • transition metal