4.3 Article

Cross-coupling Reaction of Aryl(triethyl)silanes with Aryl Chlorides: An Easy Access to Oligothiophenes

Journal

CHEMISTRY LETTERS
Volume 48, Issue 4, Pages 361-363

Publisher

CHEMICAL SOC JAPAN
DOI: 10.1246/cl.181018

Keywords

Cross-coupling; Oligothiophene; Silicon

Funding

  1. JST, ACT-C [JPMJCR12Z1]
  2. JSPS [18J12593, 17K19127]
  3. Grants-in-Aid for Scientific Research [17K19127, 18J12593] Funding Source: KAKEN

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Aryl(triethyl) silanes were found to cross-couple with aryl chlorides by palladium/copper dual catalysis and XPhos as a crucial ligand. The catalyst system is applicable to a facile oligothiophene synthesis from thienyl(trialkyl) silanes and thienyl chlorides. As the starting silanes are readily accessible by the catalytic C-H silylation, our method provides a protocol for a rapid biaryl synthesis starting with aromatic hydrocarbons straightforwardly.

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