Unimlecular Depurination of Substituted Deoxyadenosines by Fast Atom Bombardment Mass Spectrometry/Mass Spectrometry
Author:
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/07328319008045151
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2. The effect of protecting groups of the nucleobase and the sugar moieties on the acidic hydrolysis of the glycosidic bond of 2deoxyadenosine: a kinet
3. Effect of the structure of the glycon on the acid-catalyzed hydrolysis of adenine nucleosides
4. Greco, F., Liguori, A., Sindona, G. and Uccella, N. submitted for publication
5. Fast atom bombardment of solids (F.A.B.): a new ion source for mass spectrometry
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1. The structure characterization of dinucleoside and nucleoside glucopyranosides lipophilic phosphotriesters by fast-atom bombardment tandem mass spectrometry;Journal of the American Society for Mass Spectrometry;1999-10-01
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4. Deacylation of 2-N-isobutyryl- and 2-N-isobutyryl-6-O-methyl-2′-deoxyguanosine in the condensed and gas phase. A kinetic investigation;J. Chem. Soc., Perkin Trans. 2;1994
5. Fusapyrone and deoxyfusapyrone, two antifungal α-Pyrones FromFusarium semitectum;Natural Toxins;1994
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