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