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L-Phenylalaninol acts as an antiulcer agent that reduces the secretion of gastric acid and prevents ulcer formation. It inhibits intestinal absorption of L-phenylalanine making it a prospective treatment for phenylketonuria. Further, it reacts with nitriles to form oxazolines, which finds application in palladium-catalyzed allylic substitution. In addition to this, it is also used in amidation for chiral resolution and nicotinamide adenine dinucleotide modeling.
Shi, Z.; Xiao, X.; Mao, D.; Lu, G. Effects of the preparation method on the performance of the Cu/ZnO/Al2O3 catalyst for the manufacture of L-phenylalaninol with high ee selectivity from L-phenylalanine methyl ester. Catal. Sci. Technol. 2014, 4 (4), 1132-1143.
Liu, X.; Hu, L.; Jiang, L.; Jia, J.; Zhang, D.; Chen, X. Asymmetric Synthesis of Concentricolide. Eur. J. Org. Chem. 2015, 2015 (10), 2291-2296.
Gefahrenhinweise (EU): H314-H318
Causes severe skin burns and eye damage. Causes serious eye damage.
Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.