Publication | Closed Access
Novel Tunable CuX<sub>2</sub>-Mediated Cyclization Reaction of Cyclopropylideneacetic Acids and Esters for the Facile Synthesis of 4-Halomethyl-2(5<i>H</i>)-furanones and 4-Halo-5,6-dihydro-2<i>H</i>-pyran-2-ones
55
Citations
30
References
2002
Year
Asymmetric CatalysisNovel OrganocatalystsCyclopropylideneacetic AcidsEngineeringHeterocyclicBiochemistryAlkene MetathesisNatural SciencesFacile SynthesisOrganic Chemistry4-Substituted 2ChemistryHeterocycle ChemistryNatural Product SynthesisCyclization ReactionReaction TemperatureEnantioselective SynthesisBiomolecular Engineering
[reaction: see text] A mixture of cyclopropylideneacetic acids (or esters) and CuBr(2) (or CuI/I(2)) in aqueous acetonitrile afforded 4-substituted 2(5H)-furanones or 3,4-substituted 5,6-dihydro-2H-pyran-2-ones in moderate to good yields. The selectivity of the reaction greatly depended on the reaction temperature.
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