Nickel-catalysed retro-hydroamidocarbonylation of aliphatic amides to olefins
Converting the normally highly stable amide bond into different functionalities is a challenging task. Here the authors report a nickel-catalysed retro-hydroamidocarbonylation procedure, allowing the conversion of aliphatic amides into alkenes across a range of substrates.
Saved in:
| Main Authors: | , , , |
|---|---|
| Format: | article |
| Language: | EN |
| Published: |
Nature Portfolio
2017
|
| Subjects: | |
| Online Access: | https://doaj.org/article/629ee0cf137647e4abfb992fc7af714d |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | Converting the normally highly stable amide bond into different functionalities is a challenging task. Here the authors report a nickel-catalysed retro-hydroamidocarbonylation procedure, allowing the conversion of aliphatic amides into alkenes across a range of substrates. |
|---|