Direct C-H arylation of 3-methoxythiophene catalyzed by Pd. Application to a more efficient synthesis of pi-alkoxy-oligothiophene derivatives

Borghese, A.;Geldhof, G.;Antoine, L.
(2006) Tetrahedron Letters —

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  • Borghese, A.
    Author
  • Geldhof, G.
    Author
  • Antoine, L.
    Author
Abstract
The direct regioselective C-H arylation of 3-methoxythiophene and 3,4-ethylenedioxythiophene (EDOT) was performed successfully under 'Heck-type' experimental conditions. This novel synthetic methodology has been used to prepare in a more simple way a series of oligothiophenes interesting for the electronic industry to build new synthetic organic materials. (c) 2006 Elsevier Ltd. All rights reserved.
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Borghese, A., Geldhof, G., & Antoine, L. (2006). Direct C-H arylation of 3-methoxythiophene catalyzed by Pd. Application to a more efficient synthesis of pi-alkoxy-oligothiophene derivatives. Tetrahedron Letters. https://doi.org/10.1016/j.tetlet.2006.10.130