| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5263117 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
Benzaldehydes react smoothly with nonstabilized azomethine ylides, generated in situ from sarcosine/formaldehyde or N-(methoxymethyl)-N-(trimethylsilylmethyl)benzylamine, to give 5-aryloxazolidines as intermediates. These were converted into 2-(alkylamino)-1-arylethanols in good yields by simple heating in methanol with hydrochloric acid, or by treatment with hydrazine hydrate in ethanol.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Vladimir S. Moshkin, Vyacheslav Ya. Sosnovskikh,