Cargando…
Synthesis of spiro[dihydropyridine-oxindoles] via three-component reaction of arylamine, isatin and cyclopentane-1,3-dione
A fast and convenient protocol for the synthesis of novel spiro[dihydropyridine-oxindole] derivatives in satisfactory yields was developed by the three-component reactions of arylamine, isatin and cyclopentane-1,3-dione in acetic acid at room temperature. On the other hand the condensation of isatin...
Autores principales: | Sun, Yan, Sun, Jing, Yan, Chao-Guo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566796/ https://www.ncbi.nlm.nih.gov/pubmed/23399791 http://dx.doi.org/10.3762/bjoc.9.2 |
Ejemplares similares
-
Asymmetric organocatalytic Michael addition of cyclopentane-1,2-dione to alkylidene oxindole
por: Silm, Estelle, et al.
Publicado: (2022) -
Auto‐Tandem Catalysis: Pd(II)‐Catalysed Dehydrogenation/Oxidative Heck Reaction of Cyclopentane‐1,3‐diones
por: Lamb, Claire J. C., et al.
Publicado: (2017) -
Allylation of isatin-derived N-Boc-hydrazones followed by Pd-catalyzed carboamination reaction: an entry to 3-spiro-pyrazolidyl-oxindoles
por: Gazzotti, Stefano, et al.
Publicado: (2019) -
Asymmetric Synthesis of Fully Substituted Cyclopentane-Oxindoles through an Organocatalytic Triple Michael Domino Reaction
por: Zou, Liang-Hua, et al.
Publicado: (2015) -
A facile approach to spiro[dihydrofuran-2,3'-oxindoles] via formal [4 + 1] annulation reaction of fused 1H-pyrrole-2,3-diones with diazooxindoles
por: Topanov, Pavel A, et al.
Publicado: (2022)