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Catalytic Asymmetric Transfer Hydrogenation of trans-Chalcone Derivatives Using BINOL-derived Boro-phosphates.

Fei NaSusana S LopezAlice BeauseigneurLucas W HernandezZhuoxin SunJon C Antilla
Published in: Organic letters (2020)
Chiral phosphoric-acid-catalyzed asymmetric reductions of trans-chalcones have been investigated in this work. A BINOL-derived boro-phosphate-catalyzed asymmetric transfer hydrogenation of the carbon-carbon double bond of trans-chalcone derivatives employing borane as a hydride source was realized. This methodology provides a convenient procedure to access chiral dihydrochalone derivatives in high yields and with high enantioselectivities under mild conditions.
Keyphrases
  • room temperature
  • structure activity relationship
  • solid state
  • ionic liquid
  • capillary electrophoresis
  • minimally invasive
  • electron transfer
  • crystal structure