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首页> 外文期刊>Oriental Journal of Chemistry: An International Research Journal of Pure & Applied Chemistry >Synthesis of Precursor Imidazolium Salts for the Synthesis of N-heterocyclic Carbines Used as Ligands for the Enantioselective Preparation of Heterosteroids Compounds
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Synthesis of Precursor Imidazolium Salts for the Synthesis of N-heterocyclic Carbines Used as Ligands for the Enantioselective Preparation of Heterosteroids Compounds

机译:合成前体咪唑鎓盐,用于合成用作对映体制备杂环类固醇化合物的配体的N杂环卡宾

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摘要

The imidazolium salts 1-phenyl-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)-1H-imidazol-3-ium bromide (4), and 1-(pyrimidin-2-yl)-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)-1H-imidazol-3-ium bromide (5) were respectively prepared by coupling reaction of the precursors 1-phenyl-1H-imidazole (1) and 2-(1H-imidazol-1-yl)pyrimidine (2) with 2-(3-Bromopropyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(3). The purity of these compounds was confirmed by spectroscopic data. The NMR spectra showed all the signals and the structures were confirmed by HRMS.
机译:咪唑鎓盐1-苯基-3-(3-(4,4,5,5-四甲基-1,3,2-二氧杂硼硼烷-2-基)丙基)-1H-咪唑-3-溴化铵(4),和1-(嘧啶-2-基)-3-(3-(4,4,5,5-四甲基-1,3,2-二氧杂硼烷-2-基)丙基)-1H-咪唑-3-溴化铵(5)分别通过前体1-苯基-1H-咪唑(1)和2-(1H-咪唑-1-基)嘧啶(2)与2-(3-溴丙基)-4,4的偶联反应制备。 ,5,5-四甲基-1,3,2-二氧杂硼烷(3)。这些化合物的纯度通过光谱数据证实。 NMR谱显示所有信号,并且通过HRMS证实了结构。

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