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首页> 外文期刊>Chemical Communications >Pd(Ⅱ)-catalyzed decarboxylative acylation of phenylacetamides with α-oxocarboxylic acids via C-H bond activation
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Pd(Ⅱ)-catalyzed decarboxylative acylation of phenylacetamides with α-oxocarboxylic acids via C-H bond activation

机译:通过C-H键活化Pd(Ⅱ)催化苯乙酰胺与α-氧代羧酸的脱羧酰化

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摘要

A palladium-catalyzed decarboxylative acylation of phenylacet-amides with α-oxocarboxylik acids via C-H bond activation is described. This protocol provides efficient access to a range of ort/io-acyl phenylacetamides, which can be easily converted to 3-isochromanone derivatives. The development of new carbon-carbon bond-forming reactions continues to be an essential goal in organic chemistry. Traditional metal-catalyzed cross-coupling reactions between aryl metal reagents and aryl halides are well-established methods for the construction of C-C bonds and synthesis of complex molecules.
机译:描述了经由C-H键活化的钯催化的苯乙酰胺与α-氧代羰酸的脱羧酰化。该协议可有效访问一系列可轻松转换为3-isochromanone衍生物的叔/酰基苯基乙酰胺。新的碳-碳键形成反应的发展仍然是有机化学中的基本目标。芳基金属试剂与芳基卤化物之间的传统金属催化的交叉偶联反应是建立C-C键和合成复杂分子的公认方法。

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  • 来源
    《Chemical Communications 》 |2013年第16期| 1654-1656| 共3页
  • 作者单位

    School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea;

    School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea;

    School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea;

    School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea;

    School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea;

    School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea;

    School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea;

    School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea;

    School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea;

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