4.3 Article

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

期刊

CHEMISTRY LETTERS
卷 48, 期 4, 页码 361-363

出版社

CHEMICAL SOC JAPAN
DOI: 10.1246/cl.181018

关键词

Cross-coupling; Oligothiophene; Silicon

资金

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

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据