Abstract
In contrast to the photolysis of p-toluyl azide, photolysis of ortho- or meta-iodo substituted p-toluyl azide in the presence of nucleophilic trapping agents produced the corresponding triplet nitrene which led to the simple aniline products and not to the dehydroazepine-nucleophile adducts.
| Original language | English |
|---|---|
| Pages (from-to) | 899-902 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 30 |
| Issue number | 8 |
| DOIs | |
| State | Published - 1989 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry