| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5265735 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
1-t-Butyl- and 1-(4-methylbenzyl)-3-bromo-3-methylazetidines were prepared from the corresponding N-(2,3-dibromo-2-methylpropylidene)alkylamines and their propensity to undergo nucleophilic substitution at the 3-position by different nucleophiles was assessed, providing a convenient access to novel 3-alkoxy-, 3-aryloxy-, 3-hydroxy-, 3-cyano-, 3-carboxy-, 3-(aminomethyl)- and 3-(hydroxymethyl)azetidines.
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Authors
Sonja StankoviÄ, Matthias D'hooghe, Kourosch Abbaspour Tehrani, Norbert De Kimpe,