4.5 Article

Ferrocenephosphonates: Copper-Promoted Synthesis and Further Functionalization

Journal

SYNTHESIS-STUTTGART
Volume 54, Issue 12, Pages 2799-2815

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/a-1767-3026

Keywords

ferrocene; phosphonates; copper catalysis; cross-coupling; deprotolithiation

Funding

  1. Universite de Rennes 1, Centre National de la Recherche Scientifique (CNRS)
  2. University of Carthage
  3. Ministere de l'Enseignement Superieur et de la Recherche Scientifique (Tunisian Ministry of Higher Education and Scientific Research)
  4. Fonds Europeen de Developpement Regional (FEDER)
  5. European Regional Development Fund
  6. D8 VENTURE Bruker AXS diffractometer

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This article presents a method for the synthesis of ferrocenephosphonates and describes further functionalization through regioselective deprotolithiation and Negishi and Suzuki-Miyaura cross-coupling reactions. These findings provide important insights and foundations for organic synthesis and coordination chemistry.
Ferrocenephosphonates make up an important class of organometallic derivatives with a wide range of useful applications in organic synthesis and coordination chemistry. Here, an approach to ferro-cenephosphonates based on a copper-promoted Hirao coupling is reported. Further functionalizations based on regioselective deprotolithiation and both Negishi and Suzuki-Miyaura cross-coupling reactions are also described to reach original derivatives.

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