Abstract
In this paper we describe the chemoenzymatic synthesis of enantiopure L-2-arylthiazol-4-yl alanines starting from their racemic N-acetyl derivatives; by combining the lipase-catalysed dynamic kinetic resolution of oxazol-5(4H)-ones with a chemical and an enzymatic enantioselective hydrolytic step affording the desired products in good yields (74%-78%) and high enantiopurities (ee > 99%). The developed procedure exploits the utility of the single-walled carbon nanotubes-bound diethylaminoethanol as mild and efficient racemisation agent for the dynamic kinetic resolution of the corresponding oxazolones.
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Leonte, D., Bencze, L. C., Paizs, C., Tosa, M. I., Zaharia, V., & Dan Irimie, F. (2016). Heterocycles 36. Single-walled carbon nanotubes-bound n,n-diethyl ethanolamine as mild and efficient racemisation agent in the enzymatic DKR of 2-Arylthiazol-4-yl-alanines. Molecules, 21(1). https://doi.org/10.3390/molecules21010025
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