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Total Synthesis of (+)-Phrymarolin I from (+)-Malic Acid
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1997
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BiochemistryNatural Sciences-Malic AcidTotal SynthesisOrganic ChemistryStereoselective SynthesisChemistryPharmacologySynthetic ChemistryEnantioselective SynthesisPrevious SynthesisEasier AvailabilityNatural Product Synthesis
(+)-Phrymarolin I was stereoselectively synthesized from (R)-(+)-3-hydroxybutanolide that had been prepared from (+)-malic acid. The procedure is more efficient than our previous synthesis in terms of fewer reaction steps and the easier availability of the starting material.