Publication | Open Access
A Single Step Approach to Piperidines via Ni-Catalyzed β-Carbon Elimination
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Citations
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References
2012
Year
Excellent RegioselectivityChemical EngineeringBroad Substrate ScopeEngineeringHeterocyclicCatalytic SynthesisOrganic ChemistrySingle Step ApproachOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryHeterocycle ChemistryMolecular CatalysisPharmacologyEnantioselective SynthesisNi-phosphine Complex
An easy and expeditious route to substituted piperidines is described. A Ni-phosphine complex was used as catalyst for [4 + 2] cycloaddition of 3-azetidinone and alkynes. The reaction has broad substrate scope and affords piperidines in excellent yields and excellent regioselectivity. In the reaction of an enantiopure azetidinone, complete retention of stereochemistry was observed.
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