Kinetics for the acid-catalysed hydrolysis of O-, S- and N-bridged 5′,8-cyclonucleosides related to adenosine
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1994/P2/P29940000741
Reference17 articles.
1. Effects of cyclonucleoside formation on the rates of glycosidic hydrolyses in purine ribonucleosides
2. A novel method for the synthesis of cyclonucleosides. Synthesis of 8,5'-0-anhydro-8-oxyadenosine
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4. Studies of nucleosides and nucleotides—XLVI
5. Convenient synthesis of some purine 8,5'-imino cyclonucleosides
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1. Regioselective C–H and N–H functionalization of purine derivatives and analogues: a synthetic and mechanistic perspective;Catalysis Science & Technology;2018
2. Copper-Catalyzed Intramolecular Alkoxylation of Purine Nucleosides: One-Step Synthesis of 5′-O,8-Cyclopurine Nucleosides;The Journal of Organic Chemistry;2015-09-11
3. ChemInform Abstract: Kinetics for the Acid-Catalyzed Hydrolysis of O-, S- and N-Bridged 5′, 8-Cyclonucleosides Related to Adenosine.;ChemInform;2010-08-19
4. RECENT DEVELOPMENTS IN THE SYNTHESIS, CHEMICAL MODIFICATIONS AND BIOLOGICAL APPLICATIONS OF SULFUR MODIFIED NUCLEOSIDES, NUCLEOTIDES AND OLIGONUCLEOTIDES;Organic Preparations and Procedures International;2002-02
5. Cleavage of the Phosphodiester Bond of Uridylyl-(3′,5′)-8-Carboxymethylaminoadenosine by Hydronium, Hydroxide and Zinc(Ii) Ions: A Model Study Aimed at Elucidating the Potential of a Carboxylate Function as an Intramolecular Catalyst;Nucleosides, Nucleotides and Nucleic Acids;2000-10
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