Transition-Metal-Catalyzed Denitrative Coupling of Nitroarenes

Kei Muto, Toshimasa Okita, Junichiro Yamaguchi*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

Functionalization of arenes is a topic of central importance in diverse fields ranging from medicinal chemistry to materials science. Metal-catalyzed cross-coupling and nucleophilic aromatic substitution are among the most reliable methods to access functionalized arenes. In these reactions, haloarenes are often used as a versatile synthetic platform to introduce various functional groups. However, haloarenes are typically prepared from the corresponding nitroarenes through the classic sequence of reduction, diazotization, and halogenation. Thus, haloarene cross-coupling can become a multistep transformation overall. To avoid this lengthy sequence, the direct utilization of nitroarenes has the potential to significantly streamline synthetic processes and, therefore, has attracted attention in the chemistry community from the vantage points of atom- A nd step-economy. In this Review, we comprehensively cover advances in transition-metal-catalyzed denitrative reactions of nitroarenes.

Original languageEnglish
Pages (from-to)9856-9871
Number of pages16
JournalACS Catalysis
Volume10
Issue number17
DOIs
Publication statusPublished - 2020 Sep 4

Keywords

  • C-NOactivation
  • cross-coupling
  • ligand
  • nitroarenes
  • transition metal catalysis

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)

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