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Copper-catalyzed cross-coupling reactions: The formation of carbon-carbon and carbon-sulfur bonds.

机译:铜催化的交叉偶联反应:碳-碳和碳-硫键的形成。

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摘要

We have developed copper-catalyzed cross-coupling reactions for the formation of carbon-carbon and carbon-sulfur bonds. These newly developed methods demonstrate that the conditions of the traditional Ullmann reaction can be improved. We describe the synthesis of diarylacetylenes through the cross-coupling of aryl iodides and phenylacetylene using [Cu(phen)PPh 3Br] as the catalyst. This method is then utilized for the synthesis of 2-aryl-benzo[b]furans via a copper-catalyzed cross-coupling reaction between aryl acetylenes and 2-iodophenols and a subsequent 5-endo-dig cyclization. The formation of carbon-acetylene bonds is also extended to include vinyl iodides for the purpose of synthesizing 1,3-enynes. Due the lack of a general metal-mediated synthesis of aryl sulfides, we developed a copper-catalyzed cross-coupling reaction between aryl iodides and thiols using a catalytic amount of CuI and 2,9-dimethyl-1,10-phenanthroline as an additive. This method was also extended to include vinyl iodides for the synthesis of vinyl sulfides using [Cu(phen)(PPh3)2]NO3 as the catalyst. All of these methods afford the desired product in good to excellent yields without the use of palladium or expensive/air sensitive additives.
机译:我们已经开发了铜催化的交叉偶联反应,以形成碳-碳和碳-硫键。这些新开发的方法表明,可以改善传统乌尔曼反应的条件。我们描述了通过使用[Cu(phen)PPh 3Br]作为催化剂,通过芳基碘化物和苯基乙炔的交叉偶联来合成二芳基乙炔。然后,该方法通过芳基乙炔与2-碘苯酚之间的铜催化交叉偶联反应以及随后的5-endo-dig环化反应,用于合成2-芳基-苯并[b]呋喃。为了合成1,3-烯炔,碳-乙炔键的形成也扩展到包括碘乙烯。由于缺乏一般的金属介导的芳基硫醚合成方法,我们使用催化量的CuI和2,9-二甲基-1,10-菲咯啉作为添加剂,开发了芳基碘化物与硫醇之间的铜催化交叉偶联反应。 。该方法还扩展为包括乙烯基碘,该乙烯基碘用于使用[Cu(phen)(PPh3)2] NO3作为催化剂合成乙烯基硫化物。所有这些方法在不使用钯或昂贵/对空气敏感的添加剂的情况下以良好至极好的产率提供了所需的产物。

著录项

  • 作者

    Bates, Craig G.;

  • 作者单位

    University of Massachusetts Amherst.;

  • 授予单位 University of Massachusetts Amherst.;
  • 学科 Chemistry Organic.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 146 p.
  • 总页数 146
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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