Decarbonylative C-H coupling of azoles and aryl esters: Unprecedented nickel catalysis and application to the synthesis of muscoride A

Kazuma Amaike, Kei Muto, Junichiro Yamaguchi, Kenichiro Itami

Research output: Contribution to journalArticle

212 Citations (Scopus)

Abstract

A nickel-catalyzed decarbonylative C-H biaryl coupling of azoles and aryl esters is described. The newly developed catalytic system does not require the use of expensive metal catalysts or silver- or copper-based stoichiometric oxidants. We have successfully applied this new C-H arylation reaction to a convergent formal synthesis of muscoride A.

Original languageEnglish
Pages (from-to)13573-13576
Number of pages4
JournalJournal of the American Chemical Society
Volume134
Issue number33
DOIs
Publication statusPublished - 2012 Aug 22
Externally publishedYes

Fingerprint

Azoles
Nickel
Catalysis
Oxidants
Silver
Copper
Esters
Metals
Catalysts
muscoride A

ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Decarbonylative C-H coupling of azoles and aryl esters : Unprecedented nickel catalysis and application to the synthesis of muscoride A. / Amaike, Kazuma; Muto, Kei; Yamaguchi, Junichiro; Itami, Kenichiro.

In: Journal of the American Chemical Society, Vol. 134, No. 33, 22.08.2012, p. 13573-13576.

Research output: Contribution to journalArticle

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