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Proton Magnetic Resonance Investigation of Inversion at Tervalent Nitrogen, 6. Preparative Separations of Enantiomeric Diaziridines by Liquid Chromatography on Triacetylcellulose. Racemizations Monitored by Polarimetry and by <sup>1</sup>H NMR
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Citations
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References
1979
Year
EngineeringAbstract Enantiomeric DiaziridinesOrganic ChemistryChemistryPreparative SeparationsSeparation ScienceAnalytical ChemistryLiquid ChromatographyStereoselective SynthesisH NmrChromatographyDrug AnalysisBiochemistryChromatographic AnalysisPharmacologyEnantioselective SynthesisTervalent NitrogenMedicineActive Additives
Abstract Enantiomeric diaziridines have been partially separated by chromatography on triacetlycellulose. (−)‐ 2 , (+)‐ 4 , and (−)‐ 4 were obtained almost pure, enantiomeric purities (Table 1) being measured by 1 H NMR in the presence of optically active additives. The same procedure was tested for monitoring racemizations (Table 2) which were also studied, with higher accuracy, by polarimetry. The barriers to nitrogen inversion, converting the trans ‐diaziridines 2 and 4 into cis ‐intermediates, are compared with known Δ G ≠ values.
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