A Simple and General Route to Aryl Iodides from Arenes

  1. Barluenga, J. 1
  2. Campos, P.J. 1
  3. González, J.M. 1
  4. Asensio, G. 1
  1. 1 Universidad de Oviedo
    info

    Universidad de Oviedo

    Oviedo, España

    ROR https://ror.org/006gksa02

Journal:
Journal of the Chemical Society-Perkin Transactions n 1

ISSN: 0300-922X

Year of publication: 1984

Pages: 2623-2624

Type: Article

DOI: 10.1039/P19840002623 SCOPUS: 2-s2.0-37049102840 GOOGLE SCHOLAR

More publications in: Journal of the Chemical Society-Perkin Transactions n 1

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Abstract

Mercury(II) oxide-tetrafluproboric acid reacts vyith arenes under mild or very mild conditions to afford, after treatment with iodine in a 'one-stage' reaction, the corresponding aryl iodide. The orientation is that expected based on general aromatic substitution theory and hence the meta-iodinated derivatives of deactivated arenes are accessible.