Enantioselective hydrolysis of potent amino acid precursors 5-oxazolidinone derivatives

2001-01-01
Various 3-oxazolidinones have been enantioselectively hydrolysed using PLE and HLE. It has been observed that aromatic derivatives lead to better enantiomeric excesses (up to 91% and 78% respectively) and that PLE and HLE afford different enantiomers.
ENANTIOMER

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Citation Formats
C. Tanyeli, “Enantioselective hydrolysis of potent amino acid precursors 5-oxazolidinone derivatives,” ENANTIOMER, pp. 229–233, 2001, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/55559.