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https://doi.org/10.1016/j.tetlet.2015.07.068
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Cite Journal: Tetrahedron Letters |  Publication Date: Jul 27, 2015 |
 Citations: 23 |
Affiliation: Ural Federal University
Aromatic ketones were found to react smoothly with nonstabilized azomethine ylides, generated in situ from sarcosine/formaldehyde or N-(methoxymethyl)-N-(trimethylsilylmethyl)benzylamine, to give 5-aryloxazolidines which were converted into 2-alkylaminoethanols in moderate to good yields by heating in n-butanol with hydrochloric acid.
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