133617-46-6Relevant articles and documents
Palladium-Catalyzed Direct C2-Arylation of Benzo[ b ]thiophenes with Electron-Rich Aryl Halides: Facile Access to Thienoacene Derivatives
Ichioka, Fumiki,Itai, Yuhei,Nishii, Yuji,Miura, Masahiro
, p. 2812 - 2816 (2017/09/30)
Direct coupling reaction of benzo[ b ]thiophene and electron-rich aryl bromides was achieved under Pd 2 (dba) 3 /SPhos catalysis in the presence of NaO t -Bu. The reaction system was applied for the installation of 2-(methylthio)phenyl group onto thiophene-fused polyaromatic molecules, demonstrating facile synthesis of precursors for thienoacene derivatives.
Base-mediated intermolecular sp2 C-H bond arylation via benzyne intermediates
Truong, Thanh,Daugulis, Olafs
supporting information; experimental part, p. 4243 - 4245 (2011/06/21)
A transition-metal-free method for arylation of heterocycle and arene carbon-hydrogen bonds by aryl chlorides and fluorides has been developed. The reactions proceed via aryne intermediates and are highly regioselective with respect to the C-H bond coupling component.
A facile synthesis of benzo[b]thiophene derivatives
Watanabe,Date,Kawanishi,Akiyoshi,Furukawa
, p. 173 - 176 (2007/10/02)
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