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首页> 外文期刊>Angewandte Chemie >Regio- and Stereoselective Approach to 1,2-Di-and 1,1,2-Trisilylethenes by Cobalt-Mediated Reaction of Silyl-Substituted Dibromomethanes with Silylmethylmagnesiuni Reagents
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Regio- and Stereoselective Approach to 1,2-Di-and 1,1,2-Trisilylethenes by Cobalt-Mediated Reaction of Silyl-Substituted Dibromomethanes with Silylmethylmagnesiuni Reagents

机译:甲硅烷基取代的二溴甲烷与甲硅烷基甲基镁锡试剂的钴介导反应,对区域选择性和立体选择性合成1,2-二和1,1,2-三甲硅烷基

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摘要

Vinylsilanes are useful organometallic reagents in organic synthesis because the C(sp~2)-Si bonds undergo numerous transformations.'11 Multiply silylated ethenes are thus likely to represent platforms for a variety of highly substituted ethenes.Moreover,multiply silylated ethenes themselves attract considerable attention from the viewpoint of structural organic chemistry.'2' Despite their importance,there is a limited number of access routes to multiply silylated ethenes.Hydrosilylation of silylacetylenes'3' and bissilylation of acetylenes'4' are most convenient procedures.'5' Scheme 1 (top) shows representative approaches,for instance,to trisilyl-ethenes with three different silyl groups.However,difficulties are often encountered in such synthetic strategies in terms of regioselectivity and the occurrence of several side reactions.
机译:乙烯基硅烷是有机合成中有用的有机金属试剂,因为C(sp〜2)-Si键会经历许多转变。'11甲硅烷基化的聚醚因此可能代表各种高度取代的乙炔的平台。从结构有机化学的角度来关注。'2'尽管很重要,但是硅烷化乙烯的倍增途径仍然有限。甲硅烷基乙炔'3'的氢化硅烷化和乙炔'4'的双硅烷化是最方便的方法。'5'方案1(上图)显示了具有代表性的方法,例如,具有三个不同甲硅烷基的三甲硅烷基-乙烯。但是,在这种合成策略中,在区域选择性和发生数个副反应方面经常遇到困难。

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