Abstract
In the reaction of N-haloimides with 1-methylpyrrole, σ-substitution (addition-elimination) predominates over halogenation, when the halogen is chlorine.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2405-2408 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 29 |
| Issue number | 20 |
| DOIs | |
| State | Published - 1988 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry