Cargando…
Facile Synthesis of Functionalized Spiropyrrolizidine Oxindoles via a Three-Component Tandem Cycloaddition Reaction
An efficient synthesis of functionalized spiropyrrolizidine oxindoles via a three-component tandem cycloaddition has been achieved. This strategy can provide direct and rapid access to spiropyrrolizidine oxindoles in high yields (up to 99%) with excellent diastereoselectivities (up to 99:1 dr). The...
Autores principales: | Xie, Yong-Mei, Yao, Yu-Qin, Sun, Hong-Bao, Yan, Ting-Ting, Liu, Jie, Kang, Tai-Ran |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264231/ http://dx.doi.org/10.3390/molecules16108745 |
Ejemplares similares
-
Regio- and stereoselective synthesis of spiropyrrolidine-oxindole and bis-spiropyrrolizidine-oxindole grafted macrocycles through [3 + 2] cycloaddition of azomethine ylides
por: Prabhakaran, Perumal, et al.
Publicado: (2020) -
A formal intermolecular [4 + 1] cycloaddition reaction of 3-chlorooxindole and o-quinone methides: a facile synthesis of spirocyclic oxindole scaffolds
por: Lin, Chao, et al.
Publicado: (2021) -
Three-component synthesis of new unsymmetrical oxindoles via Friedel–Crafts type reaction
por: Ahadi, Somayeh, et al.
Publicado: (2011) -
Graphene Oxide Catalyzed Synthesis of Fused Chromeno Spiro Pyrrolidine Oxindoles via Tandem Decarboxylation and 1,3-Dipolar Cycloaddition
por: Singh, Vipin, et al.
Publicado: (2022) -
A Diastereoselective Synthesis of Dispiro[oxindole-cyclohexanone]pyrrolidines by 1,3-Dipolar Cycloaddition
por: Anis’kov, Alexander, et al.
Publicado: (2017)