Palladium-catalyzed one-pot synthesis of diazoles via tert-butyl isocyanide insertion

Org Biomol Chem. 2015 Nov 7;13(41):10402-8. doi: 10.1039/c5ob01328c.

Abstract

An efficient one-pot palladium-catalyzed reaction for the synthesis of diazoles from readily available hydrazides and aryl halide via isocyanide insertion/cyclization sequence has been developed. This methodology efficiently constructs diazoles in good to excellent yields with the advantages of wide functional group tolerance and operational simplicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azoles / chemical synthesis*
  • Azoles / chemistry
  • Catalysis
  • Cyclization
  • Molecular Structure
  • Nitriles / chemistry*
  • Organometallic Compounds / chemistry*
  • Palladium / chemistry*

Substances

  • Azoles
  • Nitriles
  • Organometallic Compounds
  • Palladium
  • tert-butyl isocyanide