Cargando…
Synthesis of 3,4-dihydro-1,8-naphthyridin-2(1H)-ones via microwave-activated inverse electron-demand Diels–Alder reactions
Substituted 3,4-dihydro-1,8-naphthyridin-2(1H)-ones have been synthesized with the inverse electron-demand Diels–Alder reaction from 1,2,4-triazines bearing an acylamino group with a terminal alkyne side chain. Alkynes were first subjected to the Sonogashira cross-coupling reaction with aryl halides...
Autores principales: | Fadel, Salah, Hajbi, Youssef, Khouili, Mostafa, Lazar, Said, Suzenet, Franck, Guillaumet, Gérald |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943289/ https://www.ncbi.nlm.nih.gov/pubmed/24605148 http://dx.doi.org/10.3762/bjoc.10.24 |
Ejemplares similares
-
Application of the Inverse-Electron-Demand Diels-Alder Reaction for Metabolic Glycoengineering
por: Haiber, Lisa Maria, et al.
Publicado: (2021) -
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) -
Organocatalytic Strategies for the Development of the Enantioselective Inverse‐electron‐demand Hetero‐Diels‐Alder Reaction
por: Laina‐Martín, Víctor, et al.
Publicado: (2021) -
Hydrolytically
Degradable PEG-Based Inverse Electron
Demand Diels–Alder Click Hydrogels
por: Dimmitt, Nathan H., et al.
Publicado: (2022)