Influence of different ionization conditions on the mass spectrometric behaviour of some fluorinated acyclic nucleoside analogs
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Analytical Chemistry
Reference11 articles.
1. Unimolecular decomposition of M+˙ and [M + H]+ species of some fluorosubstituted acyclic nucleoside analogs
2. Significant differences in site of protonation and extent of fragmentations in chemical ionization and fast atom bombardment mass spectrometry of simple bifunctional compounds. A mechanistic implication for formation of protonated molecules
3. Chemical ionization mass spectrometry of bifunctional compounds. The behaviour of bifunctional compounds on protonation
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1. Structure determination of 4-azido-2-pyrimidinone nucleoside analogs using mass spectrometry;Journal of Mass Spectrometry;1999-07
2. Metastable and Collision-activated Decomposition of Protonated Molecules of Isomeric N7- and N9-Substituted Purines in the Gas Phase;Rapid Communications in Mass Spectrometry;1997-02-15
3. The mass spectrometric behaviour of some halogen-containing epoxyethers;European Journal of Mass Spectrometry;1997
4. Fast-atom Bombardment Mass Spectrometry of Some Nucleoside Analogs;Rapid Communications in Mass Spectrometry;1996-07-15
5. Mass spectrometry of some fluorinated pyridinium N-imines;European Journal of Mass Spectrometry;1996
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