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亲核过氧二铁(III)配合物介导的化学计量醛去甲酰基化作为醛去甲酰化加氧酶的功能模型。

Stoichiometric Aldehyde Deformylation Mediated by Nucleophilic Peroxo-diiron(III) Complex as a Functional Model of Aldehyde Deformylating Oxygenase.

机构信息

Department of Chemistry, University of Pannonia, 8201, Veszprém, Hungary.

出版信息

Chemistry. 2019 Nov 13;25(63):14290-14294. doi: 10.1002/chem.201903727. Epub 2019 Oct 15.

Abstract

The reactivity of the previously reported peroxo adduct [Fe (μ-O )(MeBzim-Py) (CH CN) ] (1) (MeBzim-Py=2-(2'-pyridyl)-N-methylbenzimidazole) towards aldehyde substrates including phenylacetaldehyde (PAA), hydrocinnamaldehyde (HCA), propionaldehyde (PA), 2-phenylpropionaldehyde (PPA), cyclohexanecarboxaldehyde (CCA), and para-substituted benzaldehydes (benzoyl chlorides) has been investigated. Complex 1 proved to be a nucleophilic oxidant in aldehyde deformylation reaction. These models, including detailed kinetic and mechanistic studies, may serve as the first biomimics of aldehyde deformylating oxygenase (ADO) enzymes.

摘要

先前报道的过氧加合物 [Fe(μ-O)(MeBzim-Py)(CHCN)](1)(MeBzim-Py=2-(2'-吡啶基)-N-甲基苯并咪唑)对包括苯乙醛(PAA)、肉桂醛(HCA)、丙醛(PA)、2-苯基丙醛(PPA)、环己烷甲醛(CCA)和对取代苯甲醛(苯甲酰氯)在内的醛底物的反应性进行了研究。复合物 1 被证明是醛去甲酰基反应中的亲核氧化剂。这些模型,包括详细的动力学和机理研究,可能是醛去甲酰化氧化酶(ADO)酶的首例仿生模型。

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