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首页> 外文期刊>Journal of the American Chemical Society >Catalytic Asymmetric α-Acylation of Tertiary Amines Mediated by a Dual Catalysis Mode: N-Heterocyclic Carbene and Photoredox Catalysis
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Catalytic Asymmetric α-Acylation of Tertiary Amines Mediated by a Dual Catalysis Mode: N-Heterocyclic Carbene and Photoredox Catalysis

机译:双胺介导的叔胺催化不对称α-酰化反应:N-杂环碳烯和光氧化还原催化

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摘要

Cross-coupling reactions are among the most widely utilized methods for C-C bond formation; however, the requirement of preactivated starting materials still presents a major limitation. Methods that take direct advantage of the inherent reactivity of the C-H bond offer an efficient alternative to these methods, negating the requirement for substrate preactivation. In this process, two chemically distinct activation events culminate in the formation of the desired C-C bond with loss of H2 as the only byproduct. Herein we report the catalytic asymmetric α-acylation of tertiary amines with aldehydes facilitated by the combination of chiral N-heterocydic carbene catalysis and photoredox catalysis.
机译:交叉偶联反应是形成C-C键最广泛使用的方法之一。但是,对预活化原料的要求仍然存在主要限制。直接利用C-H键固有反应性的方法为这些方法提供了有效的替代方法,从而消除了底物预活化的要求。在此过程中,两个化学上不同的激活事件最终导致所需的C-C键形成,而唯一的副产物H2损失了。在本文中,我们报道了手性N-杂环卡宾催化和光氧化还原催化的组合促进了叔胺与醛的催化不对称α-酰化反应。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第19期|p.8094-8097|共4页
  • 作者单位

    Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523, United States;

    Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523, United States;

  • 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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