Login / Signup

Stereoselective Michael additions on α-aminoacrylates as the key step to an l-Oic analogue bearing a quaternary stereocenter.

Federico Maria CecchinelliGiuseppe CelentanoAlessandra PuglisiNicoletta Gaggero
Published in: Organic & biomolecular chemistry (2020)
A novel, highly stereoselective route for pharmaceutically relevant octahydroindole-2-carboxylates bearing a quaternary stereocenter has been developed. The key chiral intermediates 3 have been prepared in good yields and enantiomeric excesses up to 98%. A broad substrate range has been tolerated under the reaction conditions.
Keyphrases
  • capillary electrophoresis
  • ionic liquid
  • mass spectrometry