articleJournal of the American Chemical SocietyOct 24, 2002Closed access

Iron-Catalyzed Cross-Coupling Reactions

Max-Planck-Institut für Kohlenforschung

PubMed
Indexed incrossrefpubmed

Abstract

Simple iron salts such as FeCl(n), Fe(acac)(n) (n = 2,3) or the salen complex 4 turned out to be highly efficient, cheap, toxicologically benign, and environmentally friendly precatalysts for a host of cross-coupling reactions of alkyl or aryl Grignard reagents, zincates, or organomanganese species with aryl and heteroaryl chlorides, triflates, and even tosylates. An "inorganic Grignard reagent" of the formal composition [Fe(MgX)(2)] prepared in situ likely constitutes the propagating species responsible for the catalytic turnover, which occurs in many cases at an unprecedented rate even at or below room temperature. Because of the exceptionally mild reaction conditions, a series of functional groups such as…

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Authors

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Topics & keywords

Keywords
  • Chemistry
  • Catalysis
  • Coupling reaction
  • Coupling (piping)
  • Computational chemistry
  • Organic chemistry
  • Metallurgy
UN Sustainable Development Goals
  • Life below water
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