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Lanthanum-Catalyzed Enantioselective Trifluoromethylation by Using an Electrophilic Hypervalent Iodine Reagent.

Albert GranadosIván RivillaFernando P CossíoAdelina Vallribera
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2019)
A highly enantioselective catalytic method for the synthesis of quaternary α-trifluoromethyl derivatives of 3-oxo esters is described. The reaction uses lanthanum(III) triflate and chiral PyBOX-type C2 -symmetric ligands to generate intermediate LaIII complexes that incorporate an enolate moiety of the starting 3-oxo ester and the trifluoromethylation transfer reagent. The enantioselectivity of the reaction stems from the efficient blockage of one of the prochiral faces of the LaIII enolate by one unit of the C2 -symmetric ligand.
Keyphrases
  • electron transfer
  • room temperature
  • magnetic resonance imaging
  • mass spectrometry
  • dual energy
  • crystal structure