Cargando…
Asymmetric Synthesis of Fully Substituted Cyclopentane-Oxindoles through an Organocatalytic Triple Michael Domino Reaction
An efficient, highly stereoselective asymmetric synthesis of fully functionalized cyclopentanes bearing an oxindole moiety and several other functional groups in one pot has been developed. Key step is an organocatalytic triple Michael domino reaction forming three C–C bonds and six stereocenters, i...
Autores principales: | Zou, Liang-Hua, Philipps, Arne R, Raabe, Gerhard, Enders, Dieter |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648040/ https://www.ncbi.nlm.nih.gov/pubmed/25470781 http://dx.doi.org/10.1002/chem.201406047 |
Ejemplares similares
-
Asymmetric organocatalytic Michael addition of cyclopentane-1,2-dione to alkylidene oxindole
por: Silm, Estelle, et al.
Publicado: (2022) -
An Asymmetric Organocatalytic Quadruple Domino Reaction Employing a Vinylogous Friedel–Crafts/Michael/Michael/Aldol Condensation Sequence
por: Philipps, Arne R., et al.
Publicado: (2015) -
Asymmetric Synthesis of Tetrahydropyridines via an
Organocatalytic One-Pot Multicomponent Michael/Aza-Henry/Cyclization
Triple Domino Reaction
por: Blümel, Marcus, et al.
Publicado: (2014) -
Organocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o-Formyl-β-nitrostyrenes
por: Mahajan, Suruchi, et al.
Publicado: (2015) -
Asymmetric synthesis of cyclopentanes bearing four contiguous stereocenters via an NHC-catalyzed Michael/Michael/esterification domino reaction
por: Shu, Tao, et al.
Publicado: (2016)