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Formal [5+3] Cycloaddition of Zwitterionic Allylpalladium Intermediates with Azomethine Imines for Construction of N,O‐Containing Eight‐Membered Heterocycles
118
Citations
55
References
2017
Year
Chemical EngineeringZwitterionic Allylpalladium IntermediatesAzomethine IminesEngineeringVinylethylene CarbonatesCross-coupling ReactionZwitterionic AllylpalladiumNatural SciencesDiversity-oriented SynthesisHeterocyclicO‐containing Eight‐membered HeterocyclesOrganic ChemistryOrganometallic CatalysisCatalysisChemistryHeterocycle Chemistry
Abstract A formal [5+3] cycloaddition of zwitterionic allylpalladium intermediates with 1,3‐dipoles is developed, providing N,O‐containing eight‐membered heterocyclic compounds in high yields. Catalytically generated zwitterionic allylpalladium intermediates in situ from vinylethylene carbonates or vinyloxiranes acted as dipolarophile. magnified image
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