Design and application of α-ketothioesters as 1,2-dicarbonyl-forming reagents
Conventionally, 1,2-dicarbonyl compounds are prepared via α-keto acyl chlorides. Here, the authors report a metal-free synthesis of α-ketothioester reagents via the combination of an α-hydroxyl ketone, elemental sulfur and a benzyl halide, which are used for N- or C-dicarbonyl bond formation.
Guardado en:
| Autores principales: | , , |
|---|---|
| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
Nature Portfolio
2019
|
| Materias: | |
| Acceso en línea: | https://doaj.org/article/878544c6eb8c4e43a2d54ddad2779b72 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
| Sumario: | Conventionally, 1,2-dicarbonyl compounds are prepared via α-keto acyl chlorides. Here, the authors report a metal-free synthesis of α-ketothioester reagents via the combination of an α-hydroxyl ketone, elemental sulfur and a benzyl halide, which are used for N- or C-dicarbonyl bond formation. |
|---|