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Iridium-catalyzed stereoselective [3+2] annulation of α-oxocarboxylic acids with 1,3-dienes.

Ryota YabeYusuke EbeTakahiro Nishimura
Published in: Chemical communications (Cambridge, England) (2021)
The stereoselective annulation of α-oxocarboxylic acids with 1,3-dienes proceeded in the presence of a hydroxoiridium catalyst to give α-hydroxy-γ-lactones in good yields with high 3,5-trans relative stereochemistry. The use of a chiral diene ligand for a cationic iridium complex enabled asymmetric annulation with high enantioselectivity.
Keyphrases
  • room temperature
  • ionic liquid
  • mass spectrometry
  • carbon dioxide