Metal-free direct C-6–H alkylation of purines and purine nucleosides enabled by oxidative homolysis of 4-alkyl-1,4-dihydropyridines at room temperature
Author:
Affiliation:
1. School of Chemistry and Materials Science, Ludong University, Yantai 264025, Shandong Province, P. R. China
Abstract
Funder
National Natural Science Foundation of China
Natural Science Foundation of Shandong Province
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/OB/D2OB02070J
Reference53 articles.
1. From the website of European Medicines Agency (EMA), https://www.ema.europa.eu/en ;
2. US Food and Drug Administration (FDA), https://www.fda.gov/ , many purine and purine nucleoside drugs are easily searched
3. 6-Methylpurine, 6-Methyl-9-β-ᴅ -ribofuranosylpurine, and 6-Hydroxymethyl-9-β-D-ribofuranosylpurine as Antiviral Metabolites of Collybia maculata (Basidiomycetes)
4. Synthesis of substituted 6-cyclopropylpurine bases and nucleosides by cross-coupling reactions or cyclopropanations
5. Cytostatic and antiviral 6-arylpurine ribonucleosides. Part 7: Synthesis and evaluation of 6-substituted purine l-ribonucleosides
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2. Metal-free, direct acylation of purines to access C6-acylated purine derivatives induced by TBHP via Minisci-type reaction;New Journal of Chemistry;2024
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