Cargando…
Efficient synthesis of polyfunctionalized carbazoles and pyrrolo[3,4-c]carbazoles via domino Diels–Alder reaction
The p-TsOH-catalyzed Diels–Alder reaction of 3-(indol-3-yl)maleimides with chalcone in toluene at 60 °C afforded two diastereoisomers of tetrahydropyrrolo[3,4-c]carbazoles, which can be dehydrogenated by DDQ oxidation in acetonitrile at room temperature to give the aromatized pyrrolo[3,4-c]carbazole...
Autores principales: | Fang, Ren-Jie, Yan, Chen, Sun, Jing, Han, Ying, Yan, Chao-Guo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450976/ https://www.ncbi.nlm.nih.gov/pubmed/34621404 http://dx.doi.org/10.3762/bjoc.17.159 |
Ejemplares similares
-
Synthesis of Pyrrolo[1,2-a]pyrimidine Enantiomers via Domino Ring-Closure followed by Retro Diels-Alder Protocol
por: Fekete, Beáta, et al.
Publicado: (2017) -
HOAc-Mediated Domino Diels–Alder Reaction for
Synthesis of Spiro[cyclohexane-1,3′-indolines]
in Ionic Liquid [Bmim]Br
por: Yang, Ren-Yin, et al.
Publicado: (2018) -
Dual Activation of Aromatic Diels–Alder Reactions
por: Narsaria, Ayush K., et al.
Publicado: (2019) -
Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers
por: Nişancı, Bilal, et al.
Publicado: (2009) -
Highly selective Diels–Alder and Heck arylation reactions in a divergent synthesis of isoindolo- and pyrrolo-fused polycyclic indoles from 2-formylpyrrole
por: Escalante, Carlos H, et al.
Publicado: (2020)