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Asymmetric Linear-Selective Hydroformylation of 1,1-Dialkyl Olefins Assisted by a Steric-Auxiliary Strategy.

Dequan ZhangCai YouXiuxiu LiJialin WenXumu Zhang
Published in: Organic letters (2020)
Asymmetric hydroformylation of 1,2-dialkyl olefins was reported. In order to increase the enantiomeric induction, steric auxiliary sulfonyl groups were introduced. Using a Rh/Yanphos complex as catalyst, chiral aldehydes were obtained with high enantioselectivities under mild pressure. The easily removable auxiliary made this method a powerful tool in the preparation of important enantiopure building blocks.
Keyphrases
  • ionic liquid
  • capillary electrophoresis
  • solid state
  • room temperature
  • reduced graphene oxide
  • carbon dioxide
  • mass spectrometry