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Four-Component Reaction Access to Nitrile-Substituted All-Carbon Quaternary Centers.

Xin HuQiang BianZheng-Lin WangLin-Jie GuoYi-Ze XuGe WangDa-Zhen Xu
Published in: The Journal of organic chemistry (2021)
A four-component reaction strategy for access to acyclic nitrile-substituted all-carbon quaternary centers is disclosed. In the presence of a DABCO-based ionic liquid catalyst, the reactions proceed smoothly with a wide range of substrates efficiently to deliver nitrile-substituted all-carbon quaternary centers under mild reaction conditions. This protocol is further demonstrated as an efficient method for the construction of contiguous all-carbon quaternary centers. All the reactions are easily operated in a green manner, producing water as the only byproduct. Some of the products show excellent activity against specific fungi.
Keyphrases
  • ionic liquid
  • molecular docking
  • room temperature
  • electron transfer
  • molecular dynamics simulations
  • highly efficient
  • carbon dioxide
  • reduced graphene oxide
  • visible light
  • high density