首页> 中文期刊> 《有机化学》 >Intramolecular Biaryl Oxidative Coupling of Stilbene Substrates by Vanadium Oxytrichloride (VOCl3): Facile Synthesis of Substituted Phenanthrene Derivatives

Intramolecular Biaryl Oxidative Coupling of Stilbene Substrates by Vanadium Oxytrichloride (VOCl3): Facile Synthesis of Substituted Phenanthrene Derivatives

         

摘要

The biaryl unit is extensively presented in many classes of natural products, such as polyketides, terpenes, lignanes,coumarins, flavonoids, tannins, and many alkaloids.[1] It has long been recognized that an intramolecular oxidative phenolic or nonphenolic coupling reaction serves as the key step in the biosynthesis of these natural products, and the non-enzymic analogue of this transformation can lead the elegantly simple syntheses of these compounds.[2] During the last decade, a large number of oxidative coupling reagents, such as ferric chloride (FeCl3), phenyliodine(Ⅲ)bis(trifluoroacetate) (PIFA), lead(Ⅳ) tetraacetate [Pb(OAc)4], thallium(Ⅲ) triflouroacetate (TTFA), as well as vanadium oxytrifluoride (VOF3),[3,4] have been developed for this target. However, extensive application of this synthetic potential has been limited by low yields and unexpected side reactions usually encountered.……

著录项

  • 来源
    《有机化学》 |2004年第z1期|199|共1页
  • 作者单位

    Institute and State Key Laboratory of Elemento-Organic Chemistry;

    Nankai University;

    Tianjin 300071 Institute and State Key Laboratory of Elemento-Organic Chemistry;

    Nankai University;

    Tianjin 300071 Institute and State Key Laboratory of Elemento-Organic Chemistry;

    Nankai University;

    Tianjin 300071 Institute and State Key Laboratory of Elemento-Organic Chemistry;

    Nankai University;

    Tianjin 300071 Institute and State Key Laboratory of Elemento-Organic Chemistry;

    Nankai University;

    Tianjin 300071 Institute and State Key Laboratory of Elemento-Organic Chemistry;

    Nankai University;

    Tianjin 300071;

  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 有机化学;
  • 关键词

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