首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A novel ditopic ring-expanded N-heterocyclic carbene ligand-assisted Suzuki-Miyaura coupling reaction in aqueous media
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A novel ditopic ring-expanded N-heterocyclic carbene ligand-assisted Suzuki-Miyaura coupling reaction in aqueous media

机译:一种新型多透视环膨胀的N-杂环基石配体辅助铃木宫达水性介质偶联反应

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摘要

A series of seven-membered ditopic ring-expanded N-heterocyclic carbene (dre-NHC) precursors, bearing sterically demanding and electron-rich aryl groups, were synthesised in moderate yields via the reaction of 1,2,4,5-tetrakis(bromomethyl)benzene with the corresponding N,N'-diarylformamidines in the presence of K2CO3 in acetonitrile under an air atmosphere. All new compounds were characterised by HRMS, NMR spectroscopy, and microanalysis, as well as X-ray crystallography for compound lc. The development of an efficient catalytic system for the Suzuki-Miyaura coupling reaction of aryl chlorides with various boronic acids was also investigated using the in situ generated dre-NHC ligands. (C) 2017 Elsevier Ltd. All rights reserved.
机译:一系列七元多透视环膨胀的正杂环(DRE-NHC)前体,含有空中苛刻和富含电子的芳基,通过1,2,4,5-四左右的反应以中等产率合成( 溴甲基)苯与相应的N,N'-二芳基脒在空气气氛下在乙腈存在下的K 2 CO 3存在下。 所有新化合物的特征在于HRMS,NMR光谱和微扫描,以及化合物LC的X射线晶体。 还使用原位产生的DRE-NHC配体研究了具有各种硼酸的芳基氯化芳基氯化芳基芳基氯化物偶联反应的有效催化系统的开发。 (c)2017 Elsevier Ltd.保留所有权利。

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