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Sensitive NMR method for detecting carbohydrate influx into competing chemocatalytic pathways

机译:敏感性NMR方法检测碳水化合物流入竞争化学催化途径

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摘要

Reaction pathways are often tracked with stable isotopes in order to determine the provenance of products in the pathway and to deduce mechanistic information. NMR spectroscopy can provide direct insight into the specific labelling position of the stable isotope. We suggest a simple assay that allows rapid quantitative measurements of isotope distributions in biomass-derived products using commercially available carbohydrate substrates and routine instrumentation. In the assay, biomass-derived products in post reaction material are quantitatively reduced with NaBH4 to install hydrogens at each carbon site in the product. In this manner, the detection of ~(13)C and ~(12)C sites becomes possible in multiplets of the sensitive 2D ~1H-~1H TOCSY experiment. The approach detects the usage of competing upstream reactions from isotope patterns in chemically identical reaction products. Changing influx into Sn-Beta-catalysed carbohydrate conversion reactions in the absence and in the presence of K~+ was quantitatively assessed, showing how the presence of K~+ alters the intial reactions towards methyl lactate.
机译:通常用稳定的同位素跟踪反应途径,以便确定途径中产品的出处并推断机械信息。 NMR光谱可以直接洞察稳定同位素的特定标记位置。我们建议使用市售的碳水化合物基材和常规仪器允许快速定量测量生物量衍生产品中同位素分布的快速定量测量。在测定中,用NaBH 4定量减少后反应材料中的生物质衍生的产物,以在产品中的每个碳位点安装氢。以这种方式,在敏感2D〜1H-〜1H的多重实验中,检测〜(13)C和〜(12)C站点的检测成为可能。该方法检测在化学相同的反应产物中从同位素模式中竞争上游反应的使用。将流入流入Sn-Beta催化的碳水化合物转化反应在没有和存在K〜+的情况下定量评估,显示K〜+的存在如何改变乳酸甲酯的血液反应。

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