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CeCl<sub>3</sub>·7H<sub>2</sub>O−NaI Catalyzed Hydrooxacyclization of Unsaturated 3-Hydroxy Esters
47
Citations
21
References
2002
Year
Absolute ConfigurationEngineeringUnsaturated 3-Hydroxy EstersChloride HeptahydrateOrganic ChemistryCatalysisChemistryAcetonitrile Promote CyclizationSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
[reaction: see text] Cerium(III) chloride heptahydrate and sodium iodide in boiling acetonitrile promote cyclization of 3-hydroxyalkenoic acids esters giving 5-substituted tetrahydrofuranacetic acid esters and 6-substituted tetrahydropyranacetic acid esters in fair to good yield and with complete retention of the absolute configuration of the starting 3-hydroxy ester.
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