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Sequential Organozinc Formation and Negishi Cross-Coupling of Amides Catalysed by Cobalt Salt

  • Céline Dorval
  • , Elodie Dubois
  • , Yann Bourne-Branchu
  • , Corinne Gosmini
  • , Grégory Danoun
  • Université Paris-Saclay

Research output: Contribution to journalArticlepeer-review

26 Citations (Scopus)

Abstract

Herein, a cobalt-catalysed Negishi-type cross-coupling of amide derivatives is described. Apart from being the first example of cobalt-catalysed Negishi-type coupling of amides, the process described employs a unique, simple, and cheap catalytic system to perform both the organozinc formation and the Negishi-type coupling. Indeed, the same cobalt(II) bromide salt used to form the arylzinc species from aryl bromides is then re-used to perform the cross coupling of this resulting arylzinc with N-benzoyl glutarimides at room temperature. The main advantages of the reaction presented are its robustness and ease of use. Indeed, the reactions of organozinc formation and Negishi-type coupling are performed without precautions toward water or oxygen. (Figure presented.).

Original languageEnglish
Pages (from-to)1777-1780
Number of pages4
JournalAdvanced Synthesis and Catalysis
Volume361
Issue number8
DOIs
Publication statusPublished - 16 Apr 2019
Externally publishedYes

Keywords

  • Amides
  • Cobalt
  • Negishi-type cross-coupling
  • One-pot reaction
  • Organozinc reagent

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