A general protocol for the enantioselective synthesis of 3-heterosubstituted-2-amino-1-ols was developed based on metal- free intramolecular regio- and stereoselective diene aziridination and regioselective opening. Kinetic resolution of the resulting (1'-NR R and 1'-SR)-4-oxazolidinones was performed using ABCs organocatalysts, expanding the application of this methodology.
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| http://dx.doi.org/10.1002/chem.201902734 | DOI Listing |
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