Stereoselective intramolecular cyclization in irradiated nucleic acids: R- and S-8,5′-cycloadenosine in polyadenylic acid
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference12 articles.
1. Bildung von Cyclonucleotiden bei Bestrahlung wäßriger Lösungen von Purinnucleotiden
2. Radiation Chemistry of Nucleotides: 8,5′-Cyclonucleotide Formation and Phosphate Release Initiated by Hydroxyl Radical Attack on Adenosine Monophosphates
3. An Immunochemical Probe for 8,5′-Cycloadenosine-5′-Monophosphate and Its Deoxy Analog in Irradiated Nucleic Acids
4. Radiation-induced Decomposition of the Purine Bases within DNA and Related Model Compounds
5. Distribution of Damage in Irradiated 5′-AMP: 8,5′-Cyclo-AMP, 8-Hydroxy-AMP, and Adenine Release
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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. Structure and Stability of Duplex DNA Containing (5′S)-5′,8-Cyclo-2′-deoxyadenosine: An Oxidatively Generated Lesion Repaired by NER;Chemical Research in Toxicology;2012-09-11
4. Structures of (5′S)-8,5′-Cyclo-2′-deoxyguanosine Mismatched with dA or dT;Chemical Research in Toxicology;2012-02-06
5. Mechanisms of free radical-induced damage to DNA;Free Radical Research;2012-01-26
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