| Display title | Chemistry:Nitrone |
| Default sort key | Nitrone |
| Page length (in bytes) | 3,354 |
| Namespace ID | 3022 |
| Namespace | Chemistry |
| Page ID | 805286 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of redirects to this page | 0 |
| Counted as a content page | Yes |
| HandWiki item ID | None |
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
| Page creator | imported>Steve2012 |
| Date of page creation | 16:12, 26 June 2023 |
| Latest editor | imported>Steve2012 |
| Date of latest edit | 16:12, 26 June 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. | In organic chemistry, a nitrone is a functional group consisting of an N-oxide of an imine. The general structure is R2C=N+O−R’, where R’ is not a hydrogen. A nitrone is a 1,3-dipole, and is used in 1,3-dipolar cycloadditions. Other reactions of nitrones are known, including formal [3+3] cycloadditions... |
