Advanced Synthesis & Catalysis · 2017 · 21 citations · 72 references
Natural SciencesChemistryMedicinal ChemistryGreen ChemistryOrganic ChemistrySynthetic Medicinal ChemistryNatural Product Drug DiscoverySafer Chemical SynthesisControl ExperimentsHalogen FunctionalizationKetone FunctionalizationMedicinal Chemistry ApplicationsMild Reaction ConditionsReaction Mechanism ElucidationSubstrate Scope
Abstract α‐Halogenated ketones are both unique structure moieties existing in biologically natural products and valuable synthetic intermediates for the preparation of functional molecules. An efficient and scalable method for the preparation of α‐halogenated ketone using iron (III) chloride and iron (III) bromide as halogen sources with phenyliodonium diacetate as oxidant has been developed, featuring mild reaction conditions, environmentally friendly reagents, and wide substrate scope. Notably, the three‐step synthesis of drug prasugrel was achieved using this developed method as a key step with 30% yield on gram‐scale. Additionally, the reaction mechanism involving chloride cation was proposed based on some preliminary control experiments. magnified image
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Halogenase‐Inspired Oxidative Chlorination Using Flavin Photocatalysis
Thea Hering, Bernd Mühldorf, Robert Wolf et al. · Angewandte Chemie International Edition · 2016 · 152 citations · Full text