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Enantioselective hydrogenation of cyclic tetrasubstituted-olefinic dehydroamino acid derivatives.

Feng WanNan WangYuxin ZhuChuyan TangJerome P ClaverieWenjun Tang
Published in: Chemical communications (Cambridge, England) (2021)
An efficient asymmetric hydrogenation of cyclic tetrasubstituted-olefinic dehydroamino acid derivatives has been achieved with a Rh-ArcPhos catalyst, affording a series of α-acylamino-β-alkyl tetrahydropyranones with two contiguous chiral centers in up to 96% ee and 1000 TON.
Keyphrases
  • ionic liquid
  • structure activity relationship
  • highly efficient
  • visible light
  • mass spectrometry
  • gold nanoparticles
  • solid state