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首页> 外文期刊>The Journal of Organic Chemistry >Copper -Mediated [3+2] Oxidative Cyclization Reaction of N-Tosylhydrazones and beta-Ketoesters: Synthesis of 2,3,5-Trisubstituted Furans
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Copper -Mediated [3+2] Oxidative Cyclization Reaction of N-Tosylhydrazones and beta-Ketoesters: Synthesis of 2,3,5-Trisubstituted Furans

机译:N-甲苯磺酰hydr和β-酮酸酯的铜介导的[3 + 2]氧化环化反应:2,3,5-三取代呋喃的合成

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摘要

The first attempt at utilizing N-tosylhydrazones as two-carbon synthons has been successfully achieved, which underwent a copper-mediated [3 + 2] oxidative cyclization reaction to afford 2,3,5-trisubstituted furans in moderate to good yields. The features of this method include inexpensive metal catalyst, readily available substrates, high regioselectivity, and convenient operation. The studies provide important approaches for further exploration of the powerful and diverse reaction abilities of N-tosylhydrazones.
机译:已经成功实现了将N-甲苯磺酰as用作二碳合成子的首次尝试,该尝试进行了铜介导的[3 + 2]氧化环化反应,以中等至良好的收率提供了2,3,5-三取代的呋喃。该方法的特征包括廉价的金属催化剂,容易获得的底物,高区域选择性和方便的操作。这些研究为进一步探索N-甲苯磺酰hydr的强大而多样的反应能力提供了重要的途径。

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