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首页> 外文期刊>Journal of Molecular Structure >PEPPSI-type 2-methyl-2-propenyl-functionalized N-heterocyclic carbene-palladium complexes: Synthesis, structural characterization and catalytic activity on Suzuki-Miyaura reaction
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PEPPSI-type 2-methyl-2-propenyl-functionalized N-heterocyclic carbene-palladium complexes: Synthesis, structural characterization and catalytic activity on Suzuki-Miyaura reaction

机译:胃焦型2-甲基-2-丙烯基官能化的正杂环化钯配合物:Suzuki-miyaura反应的合成,结构表征和催化活性

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摘要

N-Heterocyclic carbenes (NHCs) have been known to be efficient ligands for the Suzuki-Miyaura cross-coupling. In this work, four novel 2-methyl-2-propenyl substituted N-heterocyclic carbene ligands (1a-d) were synthesized and they were used to produce four novel air-stable PEPPSI-type palladium-NHC complexes (2a-d). All of the new compounds were fully characterized by elemental analysis, H-1, C-13 NMR and FT-IR spectroscopies. In addition, prepared complexes (2a-d) were investigated as catalysts in the Suzuki-Miyaura coupling reaction under very mild conditions using a mixture of i-PrOH/water as a solvent and a base at the room temperature. Under optimal reaction conditions, the expected biaryl products were obtained in moderate to high yields. (C) 2018 Elsevier B.V. All rights reserved.
机译:已知N-杂环碳酸盐碳(NHC)是铃木宫亚交叉偶联的有效配体。 在这项工作中,合成了四种新的2-甲基-2-丙烯基取代的N-杂环基丙烯基配体(1A-D),用来生产四种新型空气稳定的烟头型钯-NHC络合物(2A-D)。 所有新化合物都是通过元素分析,H-1,C-13 NMR和FT-IR光谱的特征。 此外,使用I-PROH /水作为溶剂的混合物在非常温和的条件下,在非常温和的条件下,在Suzuki-Miyaura偶联反应中研究制备的配合物(2A-D)作为溶剂和室温的碱。 在最佳反应条件下,预期的前列产物中的中等至高收率。 (c)2018年elestvier b.v.保留所有权利。

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