Research output: Contribution to journal › Article › peer-review
The first example of the Büchner-Curtius-Schlotterbeck reaction of cyclic ketones with a stabilized cyclic diazo compound partner is described. The approach towards spirocyclic scaffolds has been exemplified with readily available ∝-diazo-γ-butyrolactone. The reaction proved to be viable with BF 3∙OEt 2 as the preferred catalyst and displayed substantial sensitivity to the size of the cyclic ketone.
| Original language | English |
|---|---|
| Pages (from-to) | 1800-1802 |
| Number of pages | 3 |
| Journal | Tetrahedron Letters |
| Volume | 60 |
| Issue number | 27 |
| DOIs | |
| State | Published - 4 Jul 2019 |
ID: 44840419