Chemical and Pharmaceutical Bulletin · 2000 · 17 citations · 0 references
Key StepAsymmetric CatalysisBioorganic ChemistryEnantioselective Deprotonation StrategyBiochemistryKey IntermediateNatural SciencesOrganic ChemistryFormal SynthesisStereoselective SynthesisChemistryPure FormHeterocycle ChemistryPharmacologyAntiobesity AgentSynthetic ChemistryEnantioselective SynthesisNatural Product Synthesis
Preparation of 6-substituted 4-hydroxytetrahydro-2H-pyran-2-one (12), a key intermediate for the synthesis of (-)-tetrahydrolipstatin, was achieved in an optically pure form by employing an enantioselective deprotonation reaction of the prochiral bicyclic derivative (5) as a key step.