首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >PREPARATION OF 1,4-BIS(2-ETHYNYL-3-THIENYL)BENZENES AS VERSATILE SPACERS FOR CONNECTION OF HETEROCYCLES
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PREPARATION OF 1,4-BIS(2-ETHYNYL-3-THIENYL)BENZENES AS VERSATILE SPACERS FOR CONNECTION OF HETEROCYCLES

机译:1,4-双(2-乙炔基-3-噻吩基)苯的制备作为多空间连接杂环的方法

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摘要

Iodination of 1,4-di(3-thienyl)benzene gave 1,4-bis(2-iodo-3-thienyl)-benzene,which was converted to 1,4-bis(2-ethynyl-3-thienyl)benzene.Novel 1,4-bis[2-(pyridylethynyl)-3-thienyl]benzene ligands containing the bis(ethynylthienyl)benzene spacer were prepared by Sonogashira reaction.Advantage of the spacer was demonstrated by introducing functionalized alkyl groups to the 5-position of the thiophene ring of 1,4-bis[2-(trialkylsilylethynyl)-3-thienyl]benzene.
机译:1,4-二(3-噻吩基)苯的碘化得到1,4-双(2-碘-3-噻吩基)苯,将其转化为1,4-双(2-乙炔基-3-噻吩基)苯通过Sonogashira反应制备了含有双(乙炔基噻吩基)苯间隔基的1,4-双[2-(吡啶基乙炔基)-3-噻吩基]苯配体,该间隔基的优点是通过在5-位引入官能化烷基1,4-双[2-(三烷基甲硅烷基乙炔基)-3-噻吩基]苯的噻吩环的结构。

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