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The crystal structure of the stable isomer of α-benzamidocinnamic acid: the influence of cis–trans-isomerism on the kinetics of the hydrolysis of the products of interaction of α-chymotrypsin with the isomeric 4-benzylidene-2-phenyl-Δ<sup>2</sup>-oxazolin-5-ones
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1971
Year
Crystal StructureMedicinal ChemistryEngineeringBiochemistryNatural SciencesChemical DerivativeStable IsomerOrganic ChemistrySummary X-ray AnalysisHeterocycle Chemistryα-Benzamidocinnamic AcidPharmaceutical ChemistryBiomolecular Engineering
Summary X-Ray analysis of the stable isomer of α-benzamidocinnamic acid has shown it to have the trans-configuration, a result which contradicts most previous assignments of configuration and which bears upon the properties of the products of reaction of α-chymotrypsin with the isomeric 4-benzylidene-2-phenyl-Δ2-oxazolin-5-ones.