Bulletin of the Chemical Society of Japan · 1970 · 10 citations · 2 references
Natural SciencesBiochemistryChemistryOrganic ChemistrySeparation ProcessesSpectroscopyChiral SeparationEnzyme IsolationConfigurational AnalysisConfigurational AssignmentDirect Chiral SeparationIsomer Separation AnalysisStereoisomer Separation
Abstract β-Methylnorleucine and β-methylleucine were synthesized, separated into diastereomers and optically resolved. The configurational assignments of these isomers and the determinations of the optically active isomers were achieved by means of NMR spectroscopy and the enzymatic method respectively.
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