Palladium-Catalyzed Direct C2-Arylation of Benzo[b]thiophenes with Electron-Rich Aryl Halides: Facile Access to Thienoacene Derivatives

Synlett ◽  
2017 ◽  
Vol 28 (20) ◽  
pp. 2812-2816 ◽  
Author(s):  
Fumiki Ichioka ◽  
Yuhei Itai ◽  
Yuji Nishii ◽  
Masahiro Miura

Direct coupling reaction of benzo[b]thiophene and electron-rich aryl bromides was achieved under Pd2(dba)3/SPhos catalysis in the presence of NaOt-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.

Synthesis ◽  
2012 ◽  
Vol 44 (19) ◽  
pp. 3027-3032 ◽  
Author(s):  
Yu Yuan ◽  
Ying Han ◽  
Xiaohu Wang ◽  
Xiaowei Wang ◽  
Liangzhong Lv ◽  
...  

2020 ◽  
Vol 56 (74) ◽  
pp. 10942-10945
Author(s):  
Yichao Gu ◽  
Xueliang Sun ◽  
Bin Wan ◽  
Zhuoer Lu ◽  
Yanghui Zhang

A palladium-catalyzed cross-coupling reaction of aryl halides with 2-chlorobenzoic acids has been developed through C(sp3)–H activation, which provides an innovative method for the synthesis of 9,10-dihydrophenanthren.


2018 ◽  
Vol 83 (6) ◽  
pp. 3348-3353 ◽  
Author(s):  
Yuanyong Yang ◽  
Yingxian Li ◽  
Cheng Cheng ◽  
Guo Yang ◽  
Jiquan Zhang ◽  
...  

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