Login / Signup

Asymmetric Synthesis of β-Indolyl Cyclopentanones and Cyclopentylamides with an All-Carbon Quaternary Stereocenter via Chiral Phosphoric Acid Catalyzed Friedel-Crafts Alkylation Reactions.

Wei LiuSubramani RajkumarWeihu WuZiyu HuangXiaoyu Yang
Published in: Organic letters (2019)
The asymmetric Friedel-Crafts alkylation reactions of indoles with β-substituted cyclopentenimines enabled by chiral phosphoric acid catalysis has been developed, which affords adducts possessing an all-carbon stereocenter with high levels of enantioselectivities. Furthermore, the addition products could be readily converted into two types of useful but previously challenging chiral building blocks, such as β-alkyl-β-indolyl cyclopentanones and β-alkyl-β-indolyl cyclopentylamides, in one pot via in situ hydrolysis or reduction without erosion of chiral information.
Keyphrases
  • ionic liquid
  • capillary electrophoresis
  • room temperature
  • mass spectrometry
  • healthcare
  • visible light
  • solid state