Isothiourea-Catalyzed Enantioselective Functionalisation of Glycine Schiff Base Aryl Esters via 1,6- and 1,4-Additions

Lignende værker

• Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters
  af: Shu, Chang, et al.
  Udgivet: (2019)
• Enantioselective Synthesis of α‐Aryl‐β(2)‐Amino‐Esters by Cooperative Isothiourea and Brønsted Acid Catalysis
  af: Zhao, Feng, et al.
  Udgivet: (2021)
• Nickel-catalyzed enantioselective arylation of pyridine
  af: Lutz, J. Patrick, et al.
  Udgivet: (2016)
• Ni-catalyzed asymmetric hydrogenation of N-aryl imino esters for the efficient synthesis of chiral α-aryl glycines
  af: Liu, Dan, et al.
  Udgivet: (2020)
• Ammonium Salt‐Catalyzed Ring‐Opening of Aryl‐Aziridines with β‐Keto Esters
  af: Haider, Victoria, et al.
  Udgivet: (2020)