Cargando…
Biomimetic Cationic Cyclopropanation Enables an Efficient Chemoenzymatic Synthesis of 6,8-Cycloeudesmanes
[Image: see text] Cationic cyclopropanation involves the γ-elimination at carbocations to form a new σ-C–C bond through proton loss. While exceedingly rare in bulk solution, it is recognized as one of the main biosynthetic cyclopropanation pathways. Despite the rich history of bioinspired synthetic...
Autores principales: | Grant, Phillip S., Meyrelles, Ricardo, Gajsek, Oliver, Niederacher, Gerhard, Maryasin, Boris, Maulide, Nuno |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021018/ https://www.ncbi.nlm.nih.gov/pubmed/36854118 http://dx.doi.org/10.1021/jacs.2c13116 |
Ejemplares similares
-
Redox‐Neutral Selenium‐Catalysed Isomerisation of para‐Hydroxamic Acids into para‐Aminophenols
por: Chuang, Hsiang‐Yu, et al.
Publicado: (2021) -
HFIP Mediates a Direct C−C Coupling between Michael Acceptors and Eschenmoser's salt
por: Lemmerer, Miran, et al.
Publicado: (2022) -
Direct Synthesis of α‐Amino Acid Derivatives by Hydrative Amination of Alkynes
por: Feng, Minghao, et al.
Publicado: (2022) -
Direct
Stereodivergent Olefination of Carbonyl Compounds
with Sulfur Ylides
por: Merad, Jérémy, et al.
Publicado: (2022) -
Deployment of Sulfinimines
in Charge-Accelerated Sulfonium
Rearrangement Enables a Surrogate Asymmetric Mannich Reaction
por: Feng, Minghao, et al.
Publicado: (2022)