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

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Borghese, A. Geldhof, G. Antoine, L.

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.

Document type Article de périodique (Journal article) – Article de recherche
Access type Accès restreint
Publication date 2006
Language Anglais
Journal information "Tetrahedron Letters" - Vol. 47, no. 52, p. 9249-9252 (2006)
Peer reviewed yes
Publisher Pergamon-elsevier Science Ltd (Oxford)
issn 0040-4039
e-issn 1873-3581
Affiliation UCL
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Bibliographic reference Borghese, A. ; Geldhof, G. ; Antoine, L.. Direct C-H arylation of 3-methoxythiophene catalyzed by Pd. Application to a more efficient synthesis of pi-alkoxy-oligothiophene derivatives. In: Tetrahedron Letters, Vol. 47, no. 52, p. 9249-9252 (2006)
Permanent URL http://hdl.handle.net/2078.1/37870