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ONE-POT STEREOSELECTIVE SYNTHESIS OF DIMETHY (2-HYDROXY-4,4-DIMETHYLCYCLOHEX-1-EN-6-ONE-1-YL)-3-(DIPHENYLPHOSPHONATO)BUTANEDIOATE
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References
1997
Year
Ch-acidnmr SpectroscopystereochemistryDerivative (Chemistry)EngineeringOrganic ChemistryStereoselective SynthesisReactive IntermediateChemistryAbstract ProtonationChemical DerivativeSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Abstract Protonation of the reactive intermediate produced in the reaction between triphenyl phosphite and dimethyl acetylenedicarboxylate by 5,5-dimethylcyclohexane-1,3-dione leads to vinyltriphenoxyphosphonium cation, which undergoes an addition reaction with the enolate anion of the CH-acid to produce the title compound in high yield. Key Words: Phosphonato esterTriphenyl phosphiteAcetylenic ester: CH-acidNMR spectroscopyStereochemistry
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