Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Using Amide-Based Cinchona Alkaloids as Hybrid Phase-Transfer Catalysts

Lignende værker

• Stereoselective α-Chlorination of β-Keto Esters in the Presence of Hybrid Amide-Based Cinchona Alkaloids as Catalysts
  af: Majdecki, Maciej, et al.
  Udgivet: (2020)
• Cinchona alkaloid catalyzed enantioselective amination of α,β-unsaturated ketones: an asymmetric approach to Δ(2)-pyrazolines
  af: Campbell, Nathaniel R., et al.
  Udgivet: (2011)
• Bifunctional cinchona alkaloid-squaramide-catalyzed highly enantioselective aza-Michael addition of indolines to α,β-unsaturated ketones
  af: Ghosh, Arun K., et al.
  Udgivet: (2013)
• A Peptide-Embedded Trifluoromethyl Ketone Catalyst for Enantioselective Epoxidation
  af: Romney, David K., et al.
  Udgivet: (2012)
• H-Bond Mediated Phase-Transfer Catalysis: Enantioselective Generating of Quaternary Stereogenic Centers in β-Keto Esters
  af: Patryk Niedbała, et al.
  Udgivet: (2022-04-01)