Abstract
A 1H-NMR study of the oxidative deamination of sec-alkyl primary amines with 3,5-di-tert-butyl-1,2-benzoquinone confirmed spontaneous rearrangement of the quinone-imines to the respective aromatic Schiff bases. © 1988.
| Original language | Spanish |
|---|---|
| Pages (from-to) | 851-852 |
| Number of pages | 2 |
| Journal | Tetrahedron Letters |
| Volume | 29 |
| State | Published - 1 Jan 1988 |
| Externally published | Yes |