Cargando…
Efficient synthesis of 4-sulfanylcoumarins from 3-bromo-coumarins via a highly selective DABCO-mediated one-pot thia-Michael addition/elimination process
A facile and efficient protocol for the highly selective direct sulfanylation of 3-bromocoumarins under DABCO promotion, was developed. The transformation took place with aromatic and aliphatic thiols as well as with α,ω-dithiols, affording the expected products in very good to excellent yields. Sim...
Autores principales: | Mostardeiro, Vitor B., Dilelio, Marina C., Kaufman, Teodoro S., Silveira, Claudio C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047558/ https://www.ncbi.nlm.nih.gov/pubmed/35492534 http://dx.doi.org/10.1039/c9ra09545d |
Ejemplares similares
-
Combining Silver Catalysis and Organocatalysis: A
Sequential Michael Addition/Hydroalkoxylation One-Pot Approach to
Annulated Coumarins
por: Hack, Daniel, et al.
Publicado: (2014) -
The mechanism of thia-Michael addition catalyzed by LanC enzymes
por: Ongpipattanakul, Chayanid, et al.
Publicado: (2023) -
Effect of pH on the Properties of Hydrogels Cross-Linked
via Dynamic Thia-Michael Addition Bonds
por: FitzSimons, Thomas M., et al.
Publicado: (2021) -
Thia-Michael Reaction: The Route to Promising Covalent Adaptable Networks
por: Berne, Dimitri, et al.
Publicado: (2022) -
Asymmetric synthesis of functionalized cyclohexanes bearing five stereocenters via a one-pot organocatalytic Michael–Michael–1,2-addition sequence
por: Chauhan, Pankaj, et al.
Publicado: (2014)