| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1349953 | Tetrahedron: Asymmetry | 2016 | 6 Pages |
Abstract
The SN2-like mechanism of the nucleophilic attack of sodium azide on (S)-(−)-N-acetyl-2-methoxycarbonylaziridine was verified through the chemical correlation of the ring-opening products with (S)-(+)- or (R)-(−)-2,3-diaminopropanoic acid monohydrochloride.
The SN2-like mechanism of the nucleophilic attack of sodium azide on (S)-(−)-N-acetyl-2-methoxycarbonylaziridine was verified.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Paolo Davoli, Arrigo Forni, Irene Moretti, Fabio Prati,