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 |
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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 |