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- W2038079579 abstract "The behaviour of three fluorinated acyclic nucleoside analogs has been examined under different ionization conditions, i.e. by electron ionization, fast-atom bombardment and positive-ion chemical ionization using methane, isobutane and ammonia as reactant gases. The protonated molecules have been studied by collisional spectroscopy. In general, protonation takes place on the functional groups exhibiting a proton affinity higher than that of the reactant species but some discrepancies are present. They have been explained by the presence of quasi SHF structures implicating proton bridging between sulphur and fluorine atoms." @default.
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- W2038079579 date "1995-01-01" @default.
- W2038079579 modified "2023-10-17" @default.
- W2038079579 title "Influence of different ionization conditions on the mass spectrometric behaviour of some fluorinated acyclic nucleoside analogs" @default.
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- W2038079579 doi "https://doi.org/10.1002/rcm.1290091210" @default.
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