Nucleophilic aromatic substitution using Et3SiH/cat. t-Bu-P4 as a system for nucleophile activation

Masahiro Ueno, Misato Yonemoto, Masahiro Hashimoto, Andrew E.H. Wheatley, Hiroshi Naka, Yoshinori Kondo

Research output: Contribution to journalArticlepeer-review

41 Citations (Scopus)

Abstract

A novel type of deprotonative arylation of nucleophiles was conducted using Et3SiH/cat. t-Bu-P4 and the powerful SNAr reactions of aryl fluorides were accomplished using alcohols and malonates as nucleophiles.

Original languageEnglish
Pages (from-to)2264-2266
Number of pages3
JournalChemical Communications
Issue number22
DOIs
Publication statusPublished - 2007 Jan 1

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 'Nucleophilic aromatic substitution using Et<sub>3</sub>SiH/cat. t-Bu-P4 as a system for nucleophile activation'. Together they form a unique fingerprint.

Cite this