首页> 外文期刊>Journal of the American Chemical Society >Iron-Catalyzed Dihydrosilylation of Alkynes: Efficient Access to Geminal Bis(silanes)
【24h】

Iron-Catalyzed Dihydrosilylation of Alkynes: Efficient Access to Geminal Bis(silanes)

机译:铁催化炔烃的二氢甲硅烷基化:有效获得双(硅烷)

获取原文
获取原文并翻译 | 示例
           

摘要

Geminal bis(silanes) are versatile synthetic building blocks owing to their stability and propensity to undergo a variety of transformations. However, the scarcity of catalytic methods for their synthesis limits their structural diversity and thus their utility for further applications. Herein we report a new method for synthesis of geminal bis(silanes) by means of iron-catalyzed dihydrosilylation of alkynes. Iron catalysts were distinctly superior to the other tested catalysts, which clearly demonstrates that novel reactivity can be found by using iron catalysts. This method features 100% atom economy, regiospecificity, mild reaction conditions, and readily available starting materials. Using this method, we prepared a new type of geminal bis(silane) with secondary silane moieties, the Si-H bonds of which can easily undergo various transformations, facilitating the synthetic applications of these compounds. Preliminary mechanistic studies demonstrated that the reaction proceeds via two iron-catalyzed hydrosilylation reactions, the first generating beta-(E)-vinylsilanes and the second producing geminal bis(silanes).
机译:双金属双(硅烷)由于具有稳定性和易于进行各种转化的趋势,因此是通用的合成构件。但是,催化方法缺乏用于其合成的方法限制了它们的结构多样性,因此限制了其在进一步应用中的实用性。本文中,我们报道了一种通过铁催化炔烃的二氢硅烷化来合成双(硅烷)双键的新方法。铁催化剂明显优于其他测试的催化剂,这清楚地表明,通过使用铁催化剂可以发现新的反应性。该方法具有100%的原子经济性,区域专一性,温和的反应条件和易于获得的原料。使用这种方法,我们制备了一种新型的具有仲硅烷部分的双(双)硅烷双硅烷,其Si-H键可以轻松地进行各种转化,从而促进了这些化合物的合成应用。初步的机理研究表明,该反应通过两个铁催化的氢化硅烷化反应进行,第一个生成β-(E)-乙烯基硅烷,第二个生成双键双(硅烷)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号