Photochemistry of ortho -Azidocinnamoyl Derivatives: Facile and Modular Synthesis of 2-Acylated Indoles and 2-Substituted Quinolines under Solvent Control

S. Chaabouni, N. M. Pinkerton, S. Abid, C. Galaup, S. Chassaing

Research output: Contribution to journalArticlepeer-review

Abstract

The light-promoted potential of ortho -azidocinnamoyl compounds is evaluated for heterocycle synthesis. Depending on the nature of the solvent, 2-acylated indoles were obtained under aprotic conditions, whereas the use of a protic medium led to 2-substituted quinolines. The synthetic significance of this metal-free method is that, by simply changing the solvent, the reaction outcome can be directed towards different key heterocyclic scaffolds.

Original languageEnglish (US)
Pages (from-to)2614-2618
Number of pages5
JournalSynlett
Volume28
Issue number19
DOIs
StatePublished - Dec 1 2017

Keywords

  • azides
  • indoles
  • nitrenes
  • photochemistry
  • quinolines
  • rearrangement
  • solvent effect

ASJC Scopus subject areas

  • Organic Chemistry

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