Cargando…
Engineering an Efficient and Enantioselective Enzyme for the Morita-Baylis-Hillman Reaction
The combination of computational design and directed evolution could offer a general strategy to create enzymes with new functions. To date, this approach has delivered enzymes for a handful of model reactions. Here we show that new catalytic mechanisms can be engineered into proteins to accelerate...
Autores principales: | Crawshaw, Rebecca, Crossley, Amy E., Johannissen, Linus, Burke, Ashleigh J., Hay, Sam, Levy, Colin, Baker, David, Lovelock, Sarah L., Green, Anthony P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612480/ https://www.ncbi.nlm.nih.gov/pubmed/34916595 http://dx.doi.org/10.1038/s41557-021-00833-9 |
Ejemplares similares
-
Enantioselective, Organocatalytic Morita-Baylis-Hillman and Aza-Morita-Baylis-Hillman Reactions: Stereochemical Issues
por: Mansilla, Javier, et al.
Publicado: (2010) -
Application of 7-azaisatins in enantioselective Morita–Baylis–Hillman reaction
por: He, Qing, et al.
Publicado: (2016) -
Morita–Baylis–Hillman reaction of acrylamide with isatin derivatives
por: Singh, Radhey Mohan, et al.
Publicado: (2014) -
Naphthalenes and Quinolines by Domino Reactions of Morita–Baylis–Hillman Acetates
por: Annor-Gyamfi, Joel K., et al.
Publicado: (2020) -
Dihydroquinolines, Dihydronaphthyridines and Quinolones by Domino Reactions of Morita-Baylis-Hillman Acetates
por: Annor-Gyamfi, Joel K., et al.
Publicado: (2021)