| Display title | Chemistry:Julia olefination |
| Default sort key | Julia olefination |
| Page length (in bytes) | 12,616 |
| Namespace ID | 3022 |
| Namespace | Chemistry |
| Page ID | 805833 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of redirects to this page | 1 |
| Counted as a content page | Yes |
| HandWiki item ID | None |
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
| Page creator | imported>Ohm |
| Date of page creation | 07:47, 6 March 2023 |
| Latest editor | imported>Ohm |
| Date of latest edit | 07:47, 6 March 2023 |
| Total number of edits | 1 |
| Recent number of edits (within past 90 days) | 0 |
| Recent number of distinct authors | 0 |
Description | Content |
Article description: (description)
This attribute controls the content of the description and og:description elements. | The Julia olefination (also known as the Julia–Lythgoe olefination) is the chemical reaction used in organic chemistry of phenyl sulfones (1) with aldehydes (or ketones) to give alkenes (olefins)(3) after alcohol functionalization and reductive elimination using sodium amalgam or SmI2. The reaction is... |
