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首页> 外文期刊>Journal of the American Chemical Society >Synthesis of Phenanthrone Derivatives from sec-Alkyl Aryl Ketones and Aryl Halides via a Palladium-Catalyzed Dual C-H Bond Activation and Enolate Cyclization
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Synthesis of Phenanthrone Derivatives from sec-Alkyl Aryl Ketones and Aryl Halides via a Palladium-Catalyzed Dual C-H Bond Activation and Enolate Cyclization

机译:通过钯催化的双C-H键活化和烯醇盐环化反应,由仲烷基芳基酮和芳基卤化物合成菲咯酮衍生物

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摘要

Recently, palladium-catalyzed direct transformations of inactivated C-H bonds into various functional groups has emerged as a powerful method in organic synthesis. In particular, reactions involving directing-group-assisted activation of sp or sp C-H bonds of ortho aromatic or alkenyl C-H bonds have been extensively investigated. In general, this type of ortho C-H bond activation involves a five-membered cyclometalation reaction. The directing groups frequently used in these C-H bond activation reactions include aldehyde, oxime, imine, alcohol, amine, carboxylic acid, phenol, and nitrile.
机译:最近,灭活的C-H键到各种官能团的钯催化直接转化已经成为有机合成中的一种有效方法。特别地,已经广泛研究了涉及直接芳族或烯基C-H键的sp或sp C-H键的直接基团辅助活化的反应。通常,这种邻位C-H键活化涉及五元环金属化反应。在这些C-H键活化反应中经常使用的指导基团包括醛,肟,亚胺,醇,胺,羧酸,苯酚和腈。

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  • 来源
    《Journal of the American Chemical Society 》 |2010年第25期| P.8569-8571| 共3页
  • 作者单位

    Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan;

    Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan;

    Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan;

  • 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);
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  • 正文语种 eng
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