Cargando…
Asymmetric Synthesis of [2.2.2]-Bicyclic Lactones via All-Carbon Inverse-Electron-Demand Diels–Alder Reaction
[Image: see text] In this paper, a new cycloaddition between α,β-unsaturated aldehydes and coumalates realized under dienamine activation has been described. The reaction proceeds regioselectively with the distal double bond of the dienamine system acting as electron-rich dienophile. It leads to the...
Autores principales: | Saktura, Maciej, Grzelak, Paulina, Dybowska, Joanna, Albrecht, Łukasz |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497662/ https://www.ncbi.nlm.nih.gov/pubmed/32065757 http://dx.doi.org/10.1021/acs.orglett.0c00138 |
Ejemplares similares
-
Application of the Inverse-Electron-Demand Diels-Alder Reaction for Metabolic Glycoengineering
por: Haiber, Lisa Maria, et al.
Publicado: (2021) -
Acylammonium
Salts as Dienophiles in Diels–Alder/Lactonization
Organocascades
por: Abbasov, Mikail E., et al.
Publicado: (2014) -
An intramolecular inverse electron demand Diels–Alder approach to annulated α-carbolines
por: Ma, Zhiyuan, et al.
Publicado: (2012) -
Approach Matters: The Kinetics of Interfacial Inverse‐Electron Demand Diels–Alder Reactions
por: Sen, Rickdeb, et al.
Publicado: (2017) -
Hetero-Diels–Alder reactions of hetaryl and aryl thioketones with acetylenic dienophiles
por: Mlostoń, Grzegorz, et al.
Publicado: (2015)