苯基硫代氨基脲Cu(II)配合物:室温下不同n基亲核试剂与芳基硼酸之间形成C-N键的原位催化剂

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Nibedita Gogoi, Geetika Borah, Pradip K. Gogoi
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引用次数: 3

摘要

本文报道了一种新的铜硫代氨基脲配合物催化形成C-N键的合成方法。这种原位配合物在室温下对苯胺和各种咪唑的Chan-Lam C-N交叉偶联反应非常有效。在室温下,吡唑和4-溴吲哚也被活化成C-N键。该催化体系使用DMF和水的混合物作为溶剂,以1:1的比例得到了良好到优异的收率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cu(II) complex of phenylthiosemicarbazone: An in situ catalyst for formation of C-N bond between different N-based neucleophiles with arylboronic acids at room temperature

We have reported here a new synthetic protocol for the formation of C-N bond catalyzed by a thiosemicarbazone complex of copper. This in situ complex has been found to be very effective for Chan-Lam C-N cross-coupling reaction of anilines and various imidazoles at room temperature. Pyrazole and 4-bromoindole were also activated for C-N bond formation by using this protocol at room temperature. This catalytic system gave good-to-excellent yield using a mixture of DMF and water as solvent in a 1:1 proportion.

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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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