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Lewis Acid Catalyzed Intramolecular [3+2] Cross‐Cycloaddition of Donor–Acceptor Cyclopropanes with Carbonyls: A General Strategy for the Construction of Acetal[<i>n</i>.2.1] Skeletons
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Citations
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References
2011
Year
General StrategyBioorganic ChemistryEngineering1,4-Dioxygen-substituted Cyclic SkeletonsOrganic ChemistryImportant Natural ProductsChemistryNovel OrganocatalystsMonodonor-monoacceptor CyclopropanesOrganometallic CatalysisStereoselective SynthesisBiochemistryCatalysisDonor–acceptor CyclopropanesAsymmetric CatalysisBiomolecular EngineeringHeterocyclicAlkene MetathesisNatural Sciences
Build a bridge: The first catalytic intramolecular [3+2] cycloaddition of monodonor-monoacceptor cyclopropanes (see scheme) provides a general and efficient strategy for construction of structurally diverse acetal[n.2.1] and 1,4-dioxygen-substituted cyclic skeletons, which are widely distributed in biologically important natural products.
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