Cargando…
A Facile Synthesis of Functionalized Dispirooxindole Derivatives via a Three-Component 1,3-Dipolar Cycloaddition Reaction
An efficient synthesis of novel dispirooxindoles has been achieved through three-component 1,3-dipolar cycloaddition of azomethine ylides generated in situ by the decarboxylative condensation of isatin and an α-amino acid with the dipolarophile 5-benzylideneimidazolidine-2,4-dione. The improved proc...
Autores principales: | He, Jun, Ouyang, Guang, Yuan, Zhixiang, Tong, Rongsheng, Shi, Jianyou, Ouyang, Liang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270352/ https://www.ncbi.nlm.nih.gov/pubmed/23644979 http://dx.doi.org/10.3390/molecules18055142 |
Ejemplares similares
-
An Efficient Synthesis of Novel Dispirooxindole Derivatives via One-Pot Three-Component 1,3-Dipolar Cycloaddition Reactions
por: Huang, Zhibin, et al.
Publicado: (2012) -
Molecular Hybridization-Guided One-Pot Multicomponent Synthesis of Turmerone Motif-Fused 3,3′-Pyrrolidinyl-dispirooxindoles via a 1,3-Dipolar Cycloaddition Reaction
por: Lin, Bing, et al.
Publicado: (2017) -
The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition
por: Breugst, Martin, et al.
Publicado: (2020) -
Dispirooxindole-β-Lactams: Synthesis via Staudinger Ketene-Imine Cycloaddition and Biological Evaluation
por: Filatov, Vadim E., et al.
Publicado: (2022) -
Highly Efficient and Stereoselective Construction of Bispirooxindole Derivatives via a Three-Component 1,3-Dipolar Cycloaddition Reaction
por: Xu, Qin, et al.
Publicado: (2014)