2-Hydroxyimino-6-aza-pyrimidine nucleosides: synthesis, DFT calculations, and antiviral evaluations
Author:
Affiliation:
1. Applied Nucleic Acids Research Center & Chemistry
2. Faculty of Science
3. Zagazig University
4. Zagazig
5. Egypt
6. Department of Chemistry and The RNA Institute
7. University at Albany
8. State University of New York
9. Albany
10. USA
11. Department of Medicinal Chemistry
12. Faculty of Pharmacy
Abstract
Synthesis, DFT calculations, and antiviral evaluation of a series of novel 2-hydroxyimino-6-aza-pyrimidine ribonucleosides is reported. The hydrogen bonding between the C2N–OH moiety and N3–H and/or N3 moieties shapes the pyrimidine nucleoside as purine.
Funder
National Science Foundation
Science and Technology Development Fund
National Institute of Allergy and Infectious Diseases
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2020/NJ/D0NJ04154H
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