Abstract
A tandem oxime formation/Michael addition/1,4-prototopic
shift/[3+2]-cycloaddition of an acyclic symmetrical precursor
results in a tricyclic isooxazolidine which then undergoes a further fragmentation/lactamisation cascade to generate a non-symmetrical tricyclic a-ketolactam as a single diastereomer
| Original language | English |
|---|---|
| Pages (from-to) | 2321-2324 |
| Journal | Synlett |
| Volume | 2006 |
| Issue number | 14 |
| DOIs | |
| Publication status | Published - Sept 2006 |
Keywords
- Chemistry