Wird geladen...

Rhodium catalyzed synthesis of isoindolinones via C-H activation of N-benzoylsulfonamides

An efficient approach to a wide range of isoindolinones, including 3-monosubstituted and 3,3-disubstituted isoindolinones, from the annulation of N-benzoylsulfonamides with olefins and diazoacetate has been developed. The transformation is broadly compatible with both terminal and internal olefins....

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Zhu, Chen, Falck, John R.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2012
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3472453/
https://ncbi.nlm.nih.gov/pubmed/23087489
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tet.2012.08.095
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!