Direct formation of aromatic C-N bonds. Regioselective amination of m- dinitrobenzene via fluoride promoted nucleophilic aromatic photosubstitution for hydrogen

Research output: Contribution to journalArticleResearchpeer-review

15 Citations (Scopus)

Abstract

Useful yields are achieved in the regioselective direct formation of anilines and aromatic amides through hydrogen nucleophilic aromatic photosubstitution of m-dinitrobenzene with primary amines and amides, promoted by fluoride anion.
Original languageEnglish
Pages (from-to)279-281
JournalTetrahedron Letters
Volume41
Issue number2
DOIs
Publication statusPublished - 8 Jan 2000

Keywords

  • Amination
  • Arylation
  • Nitro compounds
  • Photochemistry

Fingerprint Dive into the research topics of 'Direct formation of aromatic C-N bonds. Regioselective amination of m- dinitrobenzene via fluoride promoted nucleophilic aromatic photosubstitution for hydrogen'. Together they form a unique fingerprint.

Cite this