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A General Strategy for the Construction of Functionalized Azaindolines via Domino Palladium-Catalyzed Heck Cyclization/Suzuki Coupling.

Tabitha T SchemppBlake E DanielsSteven T StabenCraig E Stivala
Published in: Organic letters (2017)
The preparation of substituted azaindolines utilizing a domino palladium-catalyzed Heck cyclization/Suzuki coupling is described. The approach is amenable for the construction of all four azaindoline isomers. A range of functional groups such as esters, amides, ketones, sulfones, amines, and nitriles are all tolerated under the reaction conditions.
Keyphrases
  • room temperature
  • molecularly imprinted
  • electron transfer
  • molecular docking
  • mass spectrometry
  • molecular dynamics simulations