木霉酸和燕麦酸家族[13C2]-标记的植物铁载体的全合成。

IF 0.9 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of labelled compounds & radiopharmaceuticals Pub Date : 2023-09-26 DOI:10.1002/jlcr.4064
Nicolas Kratena, Markus Draskovits, Nina Biedermann, Eva Oburger, Christian Stanetty
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引用次数: 0

摘要

在此,我们报道了13个C2标记的天然产物的合成,这些产物来自木甘酸和燕麦酸家族。这些植物铁载体(“植物铁载体”)由非蛋白质氨基酸组成,在禾本科植物吸收微量营养素方面发挥着关键作用。在这项工作中,由标记的起始材料(13C2-溴乙酸,13C2-甘氨酸)制备了两个中心构建块,并进一步用于我们最近报道的提供八种同位素标记的植物铁载体的发散、分支合成策略。所需的标记构建块(13C2-l-烯丙基甘氨酸和相关的羟基化衍生物)分别通过对映选择性相转移催化和与手性助剂的对映和非对映选择性羟醛缩合制备,这两种方法本身都有潜在的价值,可用于标记(天然)产物的其他合成途径。
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Total synthesis of [13C2]-labeled phytosiderophores of the mugineic and avenic acid families

We, herein, report the synthesis of 13C2-labeled natural products from the mugineic acid and avenic acid family. These phytosiderophores (“plant iron carriers”) are built up from non-proteinogenic amino acids and play a key role in micronutrient uptake in gramineous plants. In this work, two central building blocks are prepared from labeled starting materials (13C2-bromoacetic acid, 13C2-glycine) and further employed in our recently reported divergent, branched synthetic strategy delivering eight isotopically labeled phytosiderophores. The required labeled building blocks (13C2-l-allylglycine and a related hydroxylated derivative) were prepared via enantioselective phase-transfer catalysis and enantio- and diastereoselective aldol condensation with a chiral auxiliary, respectively, both potentially valuable themselves for other synthetic routes toward labeled (natural) products.

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来源期刊
CiteScore
3.30
自引率
0.00%
发文量
57
审稿时长
1 months
期刊介绍: The Journal of Labelled Compounds and Radiopharmaceuticals publishes all aspects of research dealing with labeled compound preparation and applications of these compounds. This includes tracer methods used in medical, pharmacological, biological, biochemical and chemical research in vitro and in vivo. The Journal of Labelled Compounds and Radiopharmaceuticals devotes particular attention to biomedical research, diagnostic and therapeutic applications of radiopharmaceuticals, covering all stages of development from basic metabolic research and technological development to preclinical and clinical studies based on physically and chemically well characterized molecular structures, coordination compounds and nano-particles.
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