Kratena, N., Draskovits, M., Biedermann, N., Oburger, E., & Stanetty, C. (2023). Total synthesis of [13C₂ ]-labeled phytosiderophores of the mugineic and avenic acid families. JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 66(13), 428–434. https://doi.org/10.1002/jlcr.4064
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.