Search results for "Field desorption mass spectrometry"

showing 3 items of 3 documents

Fast atom bombardment and field desorption mass spectrometry: Comparative aspects of analytical development and bioanalytical application

1983

BioanalysisChemistryClinical BiochemistryAnalytical chemistryGeneral Materials ScienceGeneral MedicineFast atom bombardmentField desorption mass spectrometryMass spectrometryAnalytical ChemistryFresenius' Zeitschrift für analytische Chemie
researchProduct

Photodimers of cinnamic acid and related compounds. A stereochemical study by electron-impact and field desorption mass spectrometry

1974

The low energy (13 eV) electron-impact and field desorption mass spectra of some photodimers of cinnamic acid and related compounds containing the cyclobutane ring are reported and the fragmentation patterns analysed in order to obtain stereochemical information on the substituent position on the cyclobutane ring. Both symmetrical and asymmetrical splittings of the cyclobutane ring were detected, allowing characterisation of the head-to-head and head-to-tail structures of the title compounds. A ring opening rearrangement of the McLafferty type was also found.

SubstituentField desorption mass spectrometryPhotochemistryBiochemistryCinnamic acidCyclobutanechemistry.chemical_compoundchemistryFragmentation (mass spectrometry)Field desorptionMass spectrumMolecular MedicineInstrumentationSpectroscopyElectron ionizationOrganic Mass Spectrometry
researchProduct

Field Desorption Mass Spectra of Gastrine Peptides and Glutathione Derivatives

1979

Oligopeptides comprising the sequence of the C-terminal tetrapeptide of gastrine, Trp-Met-Asp-Phe-NH2, and several derivatives of glutathione, γ-Glu-Cys(SR)-Gly, were characterized by field desorption mass spectrometry. The field desorption mass spectra obtained at various field ion emitter temperatures reveal abundant molecular ions and fragmentation reactions that yield partial sequence information. In the series of glutathione derivatives investigated, characteristic ions formed by cleavage of the γ-Glu-Cys peptide bond determine the substituent at the Cys residue and can therefore be used to identify corresponding conjugation products of drug metabolites with glutathione.

chemistry.chemical_compoundChemistryField desorptionInorganic chemistryMass spectrumOrganic chemistryGeneral ChemistryGlutathioneField desorption mass spectrometryZeitschrift für Naturforschung B
researchProduct