Publication | Closed Access
Base-Controlled Selective Conversion of Michael Adducts of Malonates with Enones in the Presence of Iodine
47
Citations
38
References
2011
Year
EngineeringBiochemistryNatural SciencesMichael AdductsDiversity-oriented SynthesisOrganic ChemistryHighly Functionalized CyclopropaneStereoselective SynthesisChemistryBase-controlled Selective ConversionAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineeringα-Hydroxylmalonate Derivatives
An efficient base-controlled selective conversion of the Michael adducts of malonates with enones in the presence of iodine is reported. Highly functionalized cyclopropane, oxetane, and α-hydroxylmalonate derivatives are obtained selectively using DBU, Na(2)CO(3), and NaOAc as the base, respectively. O(2) was identified to be crucial to the formation of oxetane and α-hydroxylmalonate derivatives.
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