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首页> 外文期刊>Beilstein journal of organic chemistry. >Ring-opening reaction of 2,5-dioctyldithieno[2,3-b:3',2'-d]thiophene in the presence of aryllithium reagents
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Ring-opening reaction of 2,5-dioctyldithieno[2,3-b:3',2'-d]thiophene in the presence of aryllithium reagents

机译:在芳基锂试剂存在下2,5-二辛基二硫基[2,3-b:3',2'-d]噻吩的开环反应

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In this paper, the ring-opening reaction of 2,5-dioctyldithieno[2,3- b :3',2'- d ]thiophene with aryllithium in THF at low temperature to generate 2'-arylthio-3,3'-bithiophene-2-carbaldehydes is studied. Nine examples are explored and all the products are characterized by 1H NMR, 13C NMR and HRMS. The relative relationship between the structures of aryl groups and the efficiency of ring-opening reactions are discussed.
机译:本文研究了2,5-二辛基二硫代[2,3-b:3',2'-d]噻吩与芳基锂在THF中的低温开环反应,生成2'-芳基硫代3,3'-研究了联噻吩-2-甲醛。探索了九个实例,所有产物均通过 1 1 H NMR, 13 C NMR和HRMS表征。讨论了芳基结构与开环反应效率之间的相对关系。

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