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Template-Induced Diverse Metal-Organic Materials as Catalysts for the Tandem Acylation-Nazarov Cyclization

机译:模板诱导的多种金属有机材料作为串联酰化-纳扎罗夫环化反应的催化剂

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摘要

In our continuing quest to develop a metal-organic framework (MOF)-catalyzed tandem pyrrole acylation-Nazarov cyclization reaction with ,-unsaturated carboxylic acids for the synthesis of cyclopentenone[b]pyrroles, which are key intermediates in the synthesis of natural product (+/-)-roseophilin, a series of template-induced Zn-based (1-3) metal-organic frameworks (MOFs) have been solvothermally synthesized and characterized. Structural conversions from non-porous MOF 1 to porous MOF 2, and back to non-porous MOF 3 arising from the different concentrations of template guest have been observed. The anion- interactions between the template guests and ligands could affect the configuration of ligands and further tailor the frameworks of 1-3. Futhermore, MOFs 1-3 have shown to be effective heterogeneous catalysts for the tandem acylation-Nazarov cyclization reaction. In particular, the unique structural features of 2, including accessible catalytic sites and suitable channel size and shape, endow 2 with all of the desired features for the MOF-catalyzed tandem acylation-Nazarov cyclization reaction, including heterogeneous catalyst, high catalytic activity, robustness, and excellent selectivity. A plausible mechanism for the catalytic reaction has been proposed and the structure-reactivity relationship has been further clarified. Making use of 2 as a heterogeneous catalyst for the reaction could greatly increase the yield of total synthesis of (+/-)-roseophilin.
机译:在我们不断寻求开发金属有机骨架(MOF)催化的串联吡咯酰化-Nazarov环化反应与不饱和羧酸的合成中,用于合成环戊烯酮[b]吡咯,这是天然产物合成的关键中间体( +/-)-roseophilin,溶剂热合成和表征了一系列模板诱导的基于Zn的(1-3)金属有机骨架(MOF)。已经观察到由不同浓度的模板客体引起的从无孔MOF 1到多孔MOF 2的结构转化,以及回到无孔MOF 3的结构转化。模板客体与配体之间的阴离子相互作用可能会影响配体的构型,并进一步调整1-3的构架。此外,MOF 1-3已显示是串联酰化-Nazarov环化反应的有效多相催化剂。特别是,2的独特结构特征(包括可及的催化位点和合适的通道尺寸和形状)赋予MOF催化的串联酰化-Nazarov环化反应所需的所有特征,包括非均相催化剂,高催化活性,耐用性,并且具有出色的选择性。已经提出了催化反应的合理机理,并且进一步阐明了结构-反应性关系。使用2作为非均相催化剂进行反应可大大提高(+/-)-玫瑰果胶的全合成产率。

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