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Chiral spirocyclic phosphoric acid-catalyzed enantioselective synthesis of heterotriarylmethanes bearing an amino acid moiety.

Jin JiapingAlemayehu Gashaw WoldegiorgisXu-Feng Lin
Published in: RSC advances (2023)
We present herein an enantioselective protocol for the chiral phosphoric acid-catalyzed addition of 3-arylisoxazol-5-amines to highly reactive 3-methide-3 H -pyrroles to provide a diverse range of heterotriarylmethanes bearing an amino acid moiety in good yields (up to 97%) and high enantioselectivities (up to 93% ee) under mild conditions. The chiral spirocyclic phosphoric acid is crucial in converting the initial 1 H -pyrrol-3-yl carbinols into reactive 3-methide-3 H -pyrroles and obtaining the good enantiocontrol, thereby facilitating the desired enantioselective transformation.
Keyphrases
  • amino acid
  • ionic liquid
  • capillary electrophoresis
  • room temperature
  • randomized controlled trial