Nickel-catalysed decarbonylative borylation of aroyl fluorides

Zhenhua Wang, Xiu Wang, Yasushi Nishihara

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

The first Ni(cod)2/PPh3 catalyst system has been established for decarbonylative borylation of aroyl fluorides with bis(pinacolato)diboron. A wide range of functional groups in the substrates were well tolerated. The ease of access of the starting aroyl fluorides indicates that these results might become an alternative to the existing decarbonylation events.

Original languageEnglish
Pages (from-to)13969-13972
Number of pages4
JournalChemical Communications
Volume54
Issue number99
DOIs
Publication statusPublished - Jan 1 2018

Fingerprint

Nickel
Fluorides
Functional groups
Catalysts
Substrates
bis(pinacolato)diboron

ASJC Scopus subject areas

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Cite this

Nickel-catalysed decarbonylative borylation of aroyl fluorides. / Wang, Zhenhua; Wang, Xiu; Nishihara, Yasushi.

In: Chemical Communications, Vol. 54, No. 99, 01.01.2018, p. 13969-13972.

Research output: Contribution to journalArticle

Wang, Zhenhua ; Wang, Xiu ; Nishihara, Yasushi. / Nickel-catalysed decarbonylative borylation of aroyl fluorides. In: Chemical Communications. 2018 ; Vol. 54, No. 99. pp. 13969-13972.
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