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...

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Detalles Bibliográficos
Autores principales: Zou, Liang-Hua, Philipps, Arne R, Raabe, Gerhard, Enders, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2015
Materias:
Communications
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

Internet

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

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