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首页> 外文期刊>Journal of the American Chemical Society >Vicinal Diboronates in High Enantiomeric Purity through Tandem Site-Selective NHC-Cu-Catalyzed Boron-Copper Additions to Terminal Alkynes
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Vicinal Diboronates in High Enantiomeric Purity through Tandem Site-Selective NHC-Cu-Catalyzed Boron-Copper Additions to Terminal Alkynes

机译:通过串联位点选择性NHC-Cu催化硼铜加成到末端炔烃中的高对映体纯度的邻苯二甲酸二硼酸酯。

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摘要

We recently reported a site- and enantioselective Cu-catalyzed method for boron-copper addition to olefins carried out with bis(pina-colato)diboron [B_2(pin)_2; 1]. The transformations involve N-hetero-cyclic carbene (NHC) complexes and are performed in the presence of MeOH, which promotes in situ protonation of the C-Cu bond to regenerate the catalyst and deliver the hydroboration product.
机译:我们最近报道了用双(pina-colato)diboron [B_2(pin)_2; 1]。转化涉及N-杂环卡宾(NHC)配合物,并在MeOH的存在下进行,这可促进C-Cu键的原位质子化,从而再生催化剂并传递硼氢化产物。

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  • 来源
    《Journal of the American Chemical Society 》 |2009年第51期| 18234-18235| 共2页
  • 作者单位

    Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467;

    Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467;

    Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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