Stereoselective Synthesis of 4‘-Benzophenone-Substituted Nucleoside Analogs: Photoactive Models for Ribonucleotide Reductases
Author:
Affiliation:
1. Organisch-Chemisches Institut der Universität Heidelberg, Im Neuenheimer Feld 270, D-69120 Heidelberg, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo961372m
Reference48 articles.
1. From RNA to DNA, Why So Many Ribonucleotide Reductases?
2. Ribonucleotide reductases: radical enzymes with suicidal tendencies
3. Thiyl Radicals in Ribonucleotide Reductases
4. Ribonucleotide reductases: amazing and confusing.
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1. Synthesis of Benzophenone Nucleosides and Their Photocatalytic Evaluation for [2+2] Cycloaddition in Aqueous Media;European Journal of Organic Chemistry;2015-09-09
2. Synthesis of Iminosugars from Tetroses;Current Organic Synthesis;2014-05-31
3. Conformational control of benzophenone-sensitized charge transfer in dinucleotides;Physical Chemistry Chemical Physics;2013
4. Synthesis of a Benzophenone C-Nucleoside as Potential Triplet Energy and Charge Donor in Nucleic Acids;Synthesis;2012-01-23
5. ChemInform Abstract: Stereoselective Synthesis of 4′-Benzophenone-Substituted Nucleoside Analogues: Photoactive Models for Ribonucleotide Reductases.;ChemInform;2010-08-04
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