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Hauser–Kraus Annulation of Phthalides with Nitroalkenes for the Synthesis of Fused and Spiro Heterocycles
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Citations
50
References
2016
Year
Dieckmann CyclizationChemical EngineeringDiversity Oriented SynthesisDerivativesEngineeringHeterocyclicNatural SciencesSpiro HeterocyclesDiversity-oriented SynthesisHauser–kraus AnnulationOrganic ChemistryStrategic VariationChemistryHeterocycle ChemistryPharmacologySynthetic Chemistry
Hauser–Kraus annulation of sulfonylphthalides with simple conjugated nitroalkenes follows the expected pathway to furnish naphthoquinones in moderate yields. However, a strategic variation of this reaction by employing nitroalkenes bearing an additional nucleophilic site results in [4+4] annulation leading to complex fused and spiro heterocycles in high yields with high selectivity through a cascade process involving Michael addition, Dieckmann cyclization, and a series of eliminations and rearrangements.
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