Research output: Contribution to journal › Article › peer-review
The 1,3-dipolar cycloaddition of nitrones to N-propadienyl indoles and pyrroles proceeds predominantly via the C1-C2 bond to form 4-methyleneisoxazolidines. In the case of aldonitrones, the cis-isomers are predominantly formed.
| Original language | English |
|---|---|
| Pages (from-to) | 174-183 |
| Number of pages | 10 |
| Journal | Tetrahedron |
| Volume | 74 |
| Issue number | 1 |
| DOIs | |
| State | Published - 4 Jan 2018 |
ID: 11475082