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Indazolone‐Assisted Sequential <i>ortho</i>‐Alkenylation‐Oxidative Aza‐Michael Addition of 1‐Arylindazolone Using Acrylates Under Ru(II) Catalysis

Chikkagundagal K. Mahesha, Sanjay K. Mandal, Rajeev Sakhuja

2020Asian Journal of Organic Chemistry16 citationsDOI

Abstract

Abstract A one‐pot annulation of 1‐arylindazolones and acrylates is achieved through Ru(II)‐catalyzed sequential ortho ‐alkenylation followed by oxidative intramolecular aza‐Michael addition reaction to deliver substituted indazolo[1,2‐ a ]indazolylidenes in good‐to‐excellent yields. The strategy showcased high functional group tolerance and the directing group ability of indazolone moiety was established for Csp 2 ‐H bond activation.

Topics & Concepts

ChemistryIntramolecular forceMoietyCatalysisOxidative phosphorylationMichael reactionFunctional groupAnnulationCombinatorial chemistryMedicinal chemistryStereochemistryOrganic chemistryBiochemistryPolymerCatalytic C–H Functionalization MethodsCatalytic Cross-Coupling ReactionsSynthesis of Indole Derivatives
Indazolone‐Assisted Sequential <i>ortho</i>‐Alkenylation‐Oxidative Aza‐Michael Addition of 1‐Arylindazolone Using Acrylates Under Ru(II) Catalysis | Litcius