Nickel-catalysed denitrogenative alkyne insertion reactions of N-sulfonyl-1,2,3-triazoles

Tomoya Miura, Motoshi Yamauchi, Masahiro Murakami

Research output: Contribution to journalArticlepeer-review

197 Citations (Scopus)

Abstract

N-Sulfonyl-1,2,3-triazoles reacted with alkynes in the presence of a nickel(0)/phosphine catalyst to give substituted pyrroles, with the extrusion of molecular nitrogen; the triazole moiety isomerised to an α-imino diazo species, and the denitrogenative addition to nickel(0) was followed by the insertion of alkynes and reductive elimination.

Original languageEnglish
Pages (from-to)1470-1471
Number of pages2
JournalChemical Communications
Issue number12
DOIs
Publication statusPublished - 2009
Externally publishedYes

ASJC Scopus subject areas

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Fingerprint

Dive into the research topics of 'Nickel-catalysed denitrogenative alkyne insertion reactions of N-sulfonyl-1,2,3-triazoles'. Together they form a unique fingerprint.

Cite this