Preparation and regioselective metalation of Bis(trimethylsilyl)methyl- substituted aryl derivatives

Veronika Werner, Thomas Klatt, Masaya Fujii, Jenifer Markiewicz, Yitzhak Apeloig, Paul Knochel

Research output: Contribution to journalArticlepeer-review

Abstract

A range of bis(trimethylsilyl)methyl-substituted aryl derivatives was prepared by using a Kumada-Corriu cross-coupling reaction. The regioselective metalation of the resulting bis(trimethylsilyl)methyl-substituted aryl derivatives bearing this bulky silyl group allowed the generation of functionalized aromatics. A regioselective switch in the presence or in the absence of the bis(trimethylsilyl)methyl group has been demonstrated. Furthermore, this silyl group was converted into a formyl group or a styryl group, enhancing the scope of application of such bis(trimethylsilyl)methyl- substituted arenes.

Original languageEnglish
Pages (from-to)8338-8342
Number of pages5
JournalChemistry - A European Journal
Volume20
Issue number27
DOIs
StatePublished - 1 Jul 2014

Keywords

  • aromatics
  • lithiation
  • magnesium
  • metalation
  • silyl reagents

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Organic Chemistry

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