Login / Signup

Palladium-Copper-Catalyzed Oxidative Intermolecular [2 + 2 + 2] Coupling-Annulation: Regioselective Synthesis of Multiaryl-Substituted Benzenes.

Yihan WangBeining YangBo WangYinyin LiZhiying ZhangYatang WangWei GuoZhiyong TanLvyin Zheng
Published in: The Journal of organic chemistry (2024)
A palladium-catalyzed intermolecular [2 + 2 + 2] oxidative coupling-annulation of terminal alkenes and alkynes using copper(II) as the oxidant has been developed through direct C-C bond formation. These reactions provide effective access to multiaryl-substituted benzenes with high regioselectivity in the absence of any ligands. The features of this protocol are broad substrate scope, and high atom and step economy. The aggregation-induced emission properties of selected products were further investigated. These synthesized multiaryl-substituted benzenes may be worth exploring for further applications in the fields of advanced functional materials or drugs.
Keyphrases
  • molecular docking
  • room temperature
  • randomized controlled trial
  • electron transfer
  • molecular dynamics
  • oxide nanoparticles
  • reduced graphene oxide
  • quantum dots
  • solid state