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Aryl Coupling Reactions: Comparison
Please note this is a comparison between Version 2 by Catherine Yang and Version 1 by Helena Kang.

Aryl coupling reactions are bond-forming transformations in which an aryl fragment is joined to another molecular fragment, most commonly another aryl, alkenyl, alkynyl, alkyl, or heteroatom-bearing partner. The term includes metal-mediated and metal-catalysed processes that couple an aryl electrophile, such as an aryl halide or pseudohalide, with an organometallic or other nucleophilic partner. Their defining feature is construction of a new bond at the aromatic carbon while retaining the aryl framework. Aryl–aryl coupling is the subclass that directly joins two aryl groups [1]. Aryl iodides are especially recognised electrophilic substrates for coupling because the carbon–iodine bond can participate in catalytic activation steps [2].

  • aryl group
  • aryl halide
  • catalysis
  • carbon–carbon bond

Advanced Synthetic Organic Chemistry • Organic Chemistry • Chemistry • Physical Sciences

References

  1. K. Afarinkia; V. Vinader. Aryl Coupling Reactions; Georg Thieme Verlag KG: Stuttgart, Germany, 2003. [CrossRef]
  2. K. Iyer; J. D. Rainier. Aryl Iodide Coupling Reactions; Georg Thieme Verlag KG: Stuttgart, Germany, 2008. [CrossRef]
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