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COMBINATION OF BORANE-DIMETHYL SULFIDE COMPLEX WITH CATALYTIC SODIUM TETRAHYDROBORATE AS A SELECTIVE REDUCING AGENT FOR α-HYDROXY ESTERS. VERSATILE CHIRAL BUILDING BLOCK FROM (<i>S</i>)-(−)-MALIC ACID
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References
1984
Year
Engineeringα-Hydroxy EstersSelective Reducing AgentOrganic ChemistryCatalysisStereoselective SynthesisChemistryFour-carbon BackboneAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Abstract Borane-dimethyl sulfide complex has proven to be an efficient and selective reducing agent in the presence of catalytic sodium tetrahydroborate for α-hydroxy esters as exemplified in the reduction of dimethyl (S)-(−)-malate, providing the versatile chiral building block of four-carbon backbone.
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