Iridium-Catalyzed Asymmetric Hydrogenation of Unsaturated Piperazin-2-ones

  • Yanzhao Wang
  • , Yuanyuan Liu
  • , Kun Li
  • , Guoqiang Yang*
  • , Wanbin Zhang
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Two different iridium catalyst systems, generated from the ruthenocene-based phosphine-oxazoline ligand tBu-mono-RuPHOX or the diphosphine ligand BINAP, were developed for the asymmetric hydrogenation of 5,6-dihydropyrazin-2(1H)-ones, affording chiral piperazin-2-ones in good yields and with moderate to good ees. Different catalytic behaviors for the hydrogenation of these types of substrate were observed with these two catalyst systems. Our tBu-mono-RuPHOX ligand, which bears a ruthenocene scaffold with planar chirality, was found to be the best ligand for the [Ir(L)(COD)]BArF catalyst system, affording the desired products with up to 94% ee. (Figure presented.).

Original languageEnglish
Pages (from-to)1933-1941
Number of pages9
JournalAdvanced Synthesis and Catalysis
Volume359
Issue number11
DOIs
StatePublished - 6 Jun 2017
Externally publishedYes

Keywords

  • 3-substituted piperazin-2-ones
  • P,N ligands
  • asymmetric hydrogenation
  • cyclic imines
  • iridium

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