二糖作为底物和机制探针在接近室温的水中有效地将碳水化合物转化为甲酸

IF 4.9
Stefan S. Warthegau, Mette-Maya Siewertsen, Robert Madsen and Sebastian Meier
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引用次数: 0

摘要

甲酸盐是一种氢载体,可以在接近室温的碱性条件下用过氧化氢氧化碳水化合物。在各种可能的葡萄糖降解途径中,最相关的途径直到最近才得到澄清。生物质来源的二糖,如淀粉中的麦芽糖和纤维素中的纤维素二糖转化为甲酸酯,可以进一步支持甲酸酯的绿色生产。对于o -糖苷连接碳水化合物的转化机制、中间体、副产物和底物结构(如α-与β-键或还原端与非还原端的存在)的影响仍然知之甚少。在这里,我们缩小了这些差距,并表明化学计量量的碱和过剩的过氧化氢可以导致近定量和惊人的快速将双糖转化为甲酸中97%的有机碳。实时观察表明,葡萄糖是主要中间体,这表明稳定的葡萄糖吡喃基环中醛基团的可及性是一个限制因素。副产物包括糖基化的醛酸,它是在还原端附近由醛糖到酮糖异构化产生的。这种转化被称为Lobry de Bruyn-Van Ekenstein转化,促进了部分氧化途径,导致稳定的糖基化C10和C11酸。较高浓度的H2O2通过有利于直接氧化裂解抑制异构化,从而减少这些副产物。双糖副产物的缺失、还原性和非还原性葡萄糖氨基基残基在双糖中的几乎完全转化以及自由基清除剂的作用提供了进一步的机制理解。定量核磁共振、同位素标记和实时反应跟踪的结合,从而为二糖到甲酸酯的有效转化提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Disaccharides as substrates and mechanistic probes for efficient carbohydrate conversion to formic acid in water near room temperature

Disaccharides as substrates and mechanistic probes for efficient carbohydrate conversion to formic acid in water near room temperature

Formate is a hydrogen carrier that can be obtained by the oxidation of carbohydrates with hydrogen peroxide under aqueous alkaline conditions near room temperature. The most relevant route among various conceivable pathways for glucose degradation has only recently been clarified. The conversion of biomass-derived disaccharides such as maltose from starch and cellobiose from cellulose into formate could further support the green production of formate. The mechanism, intermediates, side products, and effect of the substrate structure (such as α- vs. β-linkages or the presence of reducing vs. non-reducing ends) remain poorly understood for the conversion of O-glycosidically linked carbohydrates. Here, we close these gaps and show that stoichiometric amounts of base and a surplus of hydrogen peroxide can lead to a near-quantitative and surprisingly rapid conversion of disaccharides to >97% organic carbon in formate. Real-time observations show that glucose is the main intermediate, indicating that the accessibility of the aldehyde groups in stable glucopyranosyl rings is a limiting factor. Side products include glycosylated aldonic acids, which derive from aldose-to-ketose isomerization near the reducing end. This transformation, known as the Lobry de Bruyn–Van Ekenstein transformation, facilitates partial oxidation pathways leading to stable glycosylated C10 and C11 acids. Higher concentrations of H2O2 suppress isomerization by favoring direct oxidative cleavage, thus minimizing these side products. The absence of disaccharide byproducts, the near-complete conversion of reducing and non-reducing glucopyranosyl residues in disaccharides, and the effect of radical scavengers provide further mechanistic understanding. The combination of quantitative NMR, isotope labeling, and real-time reaction tracking thus provides novel insight into the efficient conversion of disaccharides to formate.

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