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.
CITATION STYLE
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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