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Asymmetric Synthesis of α-Amino Acids by Organocatalytic Biomimetic Transamination.

Qi-Kai KangSermadurai SelvakumarKeiji Maruoka
Published in: Organic letters (2019)
A biomimetic enantioselective transamination of α-keto ester derivatives can be realized under mild conditions by using chiral quaternary ammonium arenecarboxylates in the absence of base additives. The corresponding α-amino acids can be used as versatile intermediates for further synthetic transformations that furnish chiral pyrrolidine and octahydroindolizine derivatives.
Keyphrases
  • amino acid
  • ionic liquid
  • capillary electrophoresis
  • structure activity relationship
  • tissue engineering
  • mass spectrometry