Publication | Closed Access
Palladium-Catalyzed Dehydrogenative Difunctionalization of Aminoalkenes with Aminals as Oxidants and Electrophiles
27
Citations
52
References
2017
Year
EngineeringOrganic ChemistryChemistrySynthetic Organic ChemistryIrritable Bowel SyndromePharmaceutical ChemistryMedicinal ChemistryOrganometallic CatalysisCross-coupling ReactionPalladium-catalyzed Dehydrogenative DifunctionalizationBiochemistryCatalysisPharmacologyAsymmetric CatalysisAminomethylation ReagentEnantioselective SynthesisBiomolecular EngineeringAlkene MetathesisNatural SciencesMolecular CatalysisSynthetic Chemistry
A novel palladium-catalyzed aminomethylamination of aminoalkenes with an aminal, functioning not only as an aminomethylation reagent but also as an oxidant, was developed. This direct and operationally simple protocol provides a fundamentally novel and unique approach toward the synthesis of 2-(2-aminoethyl)indoles and 2-(2-aminoethyl)pyrrolidines, which are important building blocks in synthetic organic chemistry. The unity of this method was highlighted by the rapid synthesis of Alosetron, a drug used for the treatment of irritable bowel syndrome.
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