Indium-mediated annulation of 2-azidoaryl aldehydes with propargyl bromides to [1,2,3]triazolo[1,5-a]quinolines

  • Xiaomin Zhang
  • , Jiali Yang
  • , Ni Xiong
  • , Zhe Han
  • , Xinhua Duan
  • , Rong Zeng

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

An efficient indium-mediated cascade annulation reaction of 2-azidoaryl aldehydes with propargyl bromides is reported. The aromatic 5/6/6-fused heterocycles, [1,2,3]triazolo[1,5-a]quinoline derivatives, could be constructed in one pot in moderate yields with a broad substrate scope. Mechanistic studies indicated that the reaction proceeded through allenol formation, azide-allene [3 + 2] cycloaddition, and dehydration. The synthetic potential of the products including the denitrogenative functionalization and the Pd-catalyzed coupling reactions has also been explored.

Original languageEnglish
Pages (from-to)6346-6352
Number of pages7
JournalOrganic and Biomolecular Chemistry
Volume19
Issue number28
DOIs
StatePublished - 28 Jul 2021

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