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Palladium-Catalyzed Desymmetric Intermolecular C-N Coupling Enabled by a Chiral Monophosphine Ligand Derived from Anthracene Photodimer.

Xin WangWei-Gang LiuLan-Tao LiuXiao-Di YangShu NiuChen-Ho TungLi-Zhu WuHuan Cong
Published in: Organic letters (2021)
The development of chiral ligands with privileged scaffolds plays an important role in transition-metal-catalyzed asymmetric reactions. Herein we present anthracene-photodimer-derived chiral monophosphine ligand 1, which features dual chirality and a rigid scaffold. This ligand exhibits remarkable efficiency in Pd-catalyzed desymmetric intermolecular C-N coupling under mild conditions with excellent chemo- and enantioselectivity.
Keyphrases
  • room temperature
  • ionic liquid
  • transition metal
  • capillary electrophoresis
  • tissue engineering
  • photodynamic therapy
  • mass spectrometry
  • energy transfer
  • radiation therapy
  • drug delivery
  • electron transfer