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首页> 外文期刊>Organic letters >Highly Selective Intra- and Intermolecular Coupling Reactions of Diazo Compounds to Form cis-Alkenes Using a Ruthenium Porphyrin Catalyst
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Highly Selective Intra- and Intermolecular Coupling Reactions of Diazo Compounds to Form cis-Alkenes Using a Ruthenium Porphyrin Catalyst

机译:重氮化合物在钌卟啉催化剂下的高选择性分子间和分子间偶联反应形成顺式烯烃

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摘要

[Ru(2,6-Cl_2TPP)(CO)] catalyzed intramolecular coupling reactions of bisdiazoacetates and intermolecular coupling reactions of monodiazoacetates to afford the coupling products in up to 76% and 93% yields, respectively. Only the cis isomers were obtained from the reactions. Employing such a ruthenium-catalyzed coupling reaction of a diazo compound as a key step allowed the synthesis of Patulolide B in 67% yield with a ratio of >40:1 against its trans isomer.
机译:[Ru(2,6-Cl_2TPP)(CO)]催化双重氮乙酸酯的分子内偶联反应和单重氮乙酸酯的分子间偶联反应,以分别提供高达76%和93%的产率的偶联产物。从反应中仅获得顺式异构体。采用重氮化合物的这种钌催化的偶联反应作为关键步骤,可以以67%的产率合成帕图洛利德B,其相对于其反式异构体的比率> 40:1。

著录项

  • 来源
    《Organic letters》 |2004年第10期|p. 1621-1623|共3页
  • 作者

    Gong-Yong Li; Chi-Ming Che;

  • 作者单位

    Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, The Chinese Academy of Sciences, 354 Feng Lin Road, Shanghai 200032, China;

    Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, The Chinese Academy of Sciences, 354 Feng Lin Road, Shanghai 200032, China;

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  • 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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