Cargando…
Dihydroquinolines, Dihydronaphthyridines and Quinolones by Domino Reactions of Morita-Baylis-Hillman Acetates
An efficient synthetic route to highly substituted dihydroquinolines and dihydronaphthyridines has been developed using a domino reaction of Morita-Baylis-Hillman (MBH) acetates with primary aliphatic and aromatic amines in DMF at 50–90 °C. The MBH substrates incorporate a side chain acetate positio...
Autores principales: | Annor-Gyamfi, Joel K., Ametsetor, Ebenezer, Meraz, Kevin, Bunce, Richard A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914960/ https://www.ncbi.nlm.nih.gov/pubmed/33567678 http://dx.doi.org/10.3390/molecules26040890 |
Ejemplares similares
-
Naphthalenes and Quinolines by Domino Reactions of Morita–Baylis–Hillman Acetates
por: Annor-Gyamfi, Joel K., et al.
Publicado: (2020) -
Enantioselective, Organocatalytic Morita-Baylis-Hillman and Aza-Morita-Baylis-Hillman Reactions: Stereochemical Issues
por: Mansilla, Javier, et al.
Publicado: (2010) -
Morita–Baylis–Hillman reaction of acrylamide with isatin derivatives
por: Singh, Radhey Mohan, et al.
Publicado: (2014) -
Application of 7-azaisatins in enantioselective Morita–Baylis–Hillman reaction
por: He, Qing, et al.
Publicado: (2016) -
Engineering an Efficient and Enantioselective Enzyme for the Morita-Baylis-Hillman Reaction
por: Crawshaw, Rebecca, et al.
Publicado: (2022)