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Efficient synthesis of highly funetionalized Indoles and Indolines by C-H bond activation

机译:通过C-H键活化有效地合成高浊度吲哚和吲哚吲哚

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Direct oxidative C-C or C-heteroatom cross-coupling by selective C-H bond activation is a promising strategy for streamlining organic synthesis and, recently, many breakthroushs have been made. In our research, we want to facilitate the synthesis of important heterocvcles bv innovative C-H bond activation reactions. Consequently, we have developed new routes to indoles and mdolines, ubiquitous motifs of biologically active natural products: - a new synthesis of highly funetionalized indoles by direct C-H bond activation of substituted anilines (Figure 1a).
机译:通过选择性C-H键活化的直接氧化C-C或C-杂原子交叉偶联是精简有机合成的有希望的策略,最近已经进行了许多突破性。在我们的研究中,我们希望促进重要的杂交BV创新的C-H键活化反应的合成。因此,我们已经为吲哚和姆多洛尔开发了新的途径,无处不在的生物活性天然产品的主题: - 通过直接C-H键活化的取代苯胺的C-H键活化来新的高浊度吲哚(图1A)。

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