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Enantioselective Oxidative Coupling of Carboxylic Acids to α-Branched Aldehydes.

Lars A LethLine NæsborgGabriel J Reyes-RodríguezHenriette N TobiesenMarc V IversenKarl Anker Jørgensen
Published in: Journal of the American Chemical Society (2018)
A new reactivity in organocatalysis is proposed to account for the coupling of carboxylic acids to α-branched aldehydes by combining primary amine catalysis and an oxidant. The developed methodology is an enantioselective α-coupling of aromatic and aliphatic carboxylic acids to α-branched aldehydes and proceeds in high yields (up to 97%) and for most examples good enantioselectivities (up to 92% ee). On the basis of experimental and mechanistic observations, the role of the primary amine catalyst is discussed.
Keyphrases
  • room temperature
  • highly efficient
  • amino acid
  • carbon dioxide