Abstract
In the presence of an oxidant, sodium iodide is converted into hypoiodous acid which effects the rearrangement of tertiary propargylic alcohols to α-iodoenones in good yields.
| Original language | English |
|---|---|
| Pages (from-to) | 8590-8592 |
| Number of pages | 3 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 10 |
| Issue number | 43 |
| Early online date | 3 Oct 2012 |
| DOIs | |
| Publication status | Published - 21 Nov 2012 |