Login / Signup

Asymmetric α-Pentadienylation of Aldehydes with Cyclopropylacetylenes.

Min-Song WuZhi-Yong HanLiu-Zhu Gong
Published in: Organic letters (2021)
By employing readily available cyclopropylacetylene and its derivatives as the pentadienylation reagent, an asymmetric regioselective asymmetric α-pentadienylation reaction of aldehydes is developed by cooperative catalysis of a chiral Pd(0) catalyst and a chiral Brønsted acid in the presence of a subschoichmetric amount of an achiral amine. α-Pentadienylated aldehydes are afforded with high yields and enantioselectivities as well as excellent E/Z ratios.
Keyphrases
  • ionic liquid
  • solid state
  • capillary electrophoresis
  • room temperature
  • highly efficient
  • metal organic framework