Journal of the American Chemical Society · 2021 · 40 citations · 55 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryChemical Library DesignDiversity-oriented SynthesisHeterocyclic ChemistryOrganic SynthesisRetrosynthetic AnalysisTarget-oriented SynthesisBorylation ReactionsC - C Coupling ReactionsLate-stage DiversificationMedicinal HeterocyclesNatural Product Total SynthesisNitrogen HeterocyclesPrecursor ChemistryPyridine Chemistry
-desmethyl-β-obscurine. Key steps in the syntheses include oxidative C-C bond cleavage of a piperidine ring in the core structure of the obscurine intermediate and site-selective C-H borylation of a pyridine nucleus to enable cross-coupling reactions.
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