| Display title | Chemistry:Cornforth rearrangement |
| Default sort key | Cornforth rearrangement |
| Page length (in bytes) | 3,868 |
| Namespace ID | 3022 |
| Namespace | Chemistry |
| Page ID | 805393 |
| Page content language | en - English |
| Page content model | wikitext |
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| Page creator | imported>Steve2012 |
| Date of page creation | 10:30, 8 February 2024 |
| Latest editor | imported>Steve2012 |
| Date of latest edit | 10:30, 8 February 2024 |
| Total number of edits | 1 |
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Description | Content |
Article description: (description)
This attribute controls the content of the description and og:description elements. | In organic chemistry, the Cornforth rearrangement is a rearrangement reaction of a 4-acyloxazole in which the group attached to an acyl on position 4 and the substituent on position 5 of an oxazole ring exchange places. It was first reported in 1949, and is named for John Cornforth. The reaction is used... |
