Publication | Closed Access
Stereochemical characterization of some mono‐ and diaryl substituted ethylene oxides by NMR spectroscopy
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Citations
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References
1970
Year
Chemical EngineeringEthylene OxidesStereochemical CharacterizationBiochemistryNmr SpectroscopyNatural SciencesEngineeringSolid-state Nmr SpectroscopyChemical ShiftsTrans IsomersSpectra-structure CorrelationOxirane ProtonsOrganic ChemistryStereoselective SynthesisChemistrySolution Nmr SpectroscopyMolecular ChemistryNuclear Magnetic Resonance Spectroscopy
Abstract NMR spectra of several styrene, stilbene and stilbazole oxides have been determined, and chemical shifts and coupling constants have been correlated with cis ‐and trans ‐configurations. Assignments have been made for all protons, and double resonance technique and 13 CH coupling constants have been used in some particular cases. An explanation is proposed for the observation that chemical shifts of oxirane protons are higher for cis than for trans isomers.
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