The Journal of Organic Chemistry · 2024 · 12 citations · 33 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisFunctional Group ToleranceIndole ChemistryIndole DerivativesIndole SynthesisRing-forming ReactionsTransformations
An efficient approach for the preparation of tetracyclic indeno[1,2- b ]indoles via Rh(III)-catalyzed C–H cascade annulation between arylhydrazines and diazo indan-1,3-diones has been established. In addition, a series of indeno[1,2- b ]indoles were obtained in up to 96% yield with a wide range of substrates and high functional group tolerance. Finally, the diverse transformations of the desired products demonstrate the synthetic utility and utilization of this protocol.
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