This website uses cookies to give you the best user experience. If you continue without changing your settings we'll assume you are happy to receive all RSC cookies. You can change your cookie settings by navigating to our Privacy and Cookies page and following the instructions. These instructions are also obtainable from the privacy link at the bottom of any RSC page.
Lite Version|Standard version
Home > Organic & Biomolecular ... >
Download
PDF
Rich HTML
Abstract | Cited by

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.

Graphical abstract: Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to α-iodoenones

Page: ^ Top


Enter Keywords, author, title,reference, or DOI
Log in | Register