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Mass spectrometry of thio analogues of pyrimidine bases: Correlation of the intensities of the M<sup>+˙</sup> and selected fragment ions of <i>o</i>‐(<i>m</i>‐ and <i>p</i>‐)substituted benzylthiouracils
17
Citations
5
References
1995
Year
EngineeringThio AnaloguesBiological Mass SpectrometryOrganic ChemistryChemistryMass Spectral FragmentationsHeterocycle ChemistryChemical DerivativeSpectra-structure CorrelationMedicinal ChemistryAnalytical ChemistryBenzyl GroupsChemical MeasurementBiochemistryNatural SciencesMass SpectrometryStructural IsomersPyrimidine BasesMolecular FragmentationDrug Analysis
Abstract The mass spectral fragmentations of sixteen new 2‐and 4‐ o ‐( m ‐ and p ‐)substituted benzylthiouracils and o ‐( m ‐ and p ‐)substituted 2,4‐dibenzylthiouracils with NO 2 and CI substituents in the benzyl groups were investigated. Fragmentation pathways are proposed on the basis of accurate mass and metastable transitions measurements. The correlation between the abundances of the M +˙ and the selected fragment ions of investigated compounds is discussed. The data obtained create the basis for distinguishing structural isomers.
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