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Carbon‐13 NMR spectroscopy of hop bitter substances
23
Citations
13
References
1975
Year
Food ChemistryH Nmr ShiftsC Nmr SpectraEngineeringBiochemistryFlavoromicsHop Bitter SubstancesSpectroscopyNatural SciencesChemical MeasurementChemical CompositionOrganic ChemistryAnalytical ChemistryCarbon AtomsChemistrySpectra-structure Correlation
Abstract The 13 C NMR spectra of the most important hop bitter substances are analysed. All individual carbon atoms are assigned, except the oxygen bonded sp 2 carbon atoms. Most assignments are made partly by comparison with analogous compounds and partly by reference to literature data. Cross‐correlations with the 1 H NMR shifts are made for two main products and confirm the correctness of the assignments. All data are in agreement with the known structures.
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1964 | 781 | |
1966 | 366 | |
1970 | 286 | |
1970 | 229 | |
1963 | 114 | |
1972 | 74 | |
1965 | 61 | |
1971 | 54 | |
1970 | 53 | |
1964 | 35 |
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