Mechanisms for the solvolytic decompositions of nucleoside analogues—VIII
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference26 articles.
1. Kinetics and mechanism of the acid-catalyzed hydrolysis of some purine nucleosides
2. Kinetics and mechanism of the hydrolysis of guanosine and 7-methylquanosine nucleosides in perchloric acid
3. Relative stability and a quantitative approach to the reaction mechanism of the acid-catalyzed hydrolysis of certain 7- and 9-.beta.-D-ribofuranosylpurines
4. Contribution to the mechanism of the acid-catalyzed hydrolysis of purine nucleosides
5. Solvolysis of adenine nucleosides. I. Effects of sugars and adenine substituents on acid solvolyses
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1. Chemical shifts and coupling constants of C7H11N3O2;Chemical Shifts and Coupling Constants for Carbon-13;2007
2. Investigation of The Kinetics of Degradation of Hexopyranosylated Cytosine Nucleosides Using Liquid Chromatography;Nucleosides, Nucleotides and Nucleic Acids;2000-01
3. Synthesis Of Nucleosides;Organic Reactions;1999-11-08
4. Kinetics for the Acid-Catalyzed Hydrolysis of Purine and Cytosine 2′-Deoxy-4′-thionucleosides;Nucleosides and Nucleotides;1999-02
5. Additional evidence for the exceptional mechanism of the acid-catalysed hydrolysis of 4-oxopyrimidine nucleosides: hydrolysis of 1-(1-alkoxyalkyl)uracils, seconucleosides, 3′-C-alkyl nucleosides and nucleoside 3′,5′-cyclic monophosphates;J. Chem. Soc., Perkin Trans. 2;1994
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