Open Access
Beilstein Journal of Organic Chemistry, volume 20, pages 2599-2607
Efficient modification of peroxydisulfate oxidation reactions of nitrogen-containing heterocycles 6-methyluracil and pyridine
Alfiya R Gimadieva
1
,
Yuliya Zulkifovna Khazimullina
1
,
Aigiza Aidarovna Gilimkhanova
1
,
Akhat G. Mustafin
1
Publication type: Journal Article
Publication date: 2024-10-16
scimago Q2
SJR: 0.517
CiteScore: 4.9
Impact factor: 2.2
ISSN: 18605397
Abstract
Nitrogen-containing heterocyclic compounds are widely used in pharmacology due to their pronounced biological activities and low toxicities. The introduction of a hydroxy function into uracil and pyridine molecules has led to compounds with antioxidant, anti-inflammatory, and immunomodulatory activity (3-hydroxy-6-methyl-2-ethylpyridine, 5-hydroxy-6-methyluracil, etc.). One of the successful methods for hydroxylation is peroxydisulfate oxidation. By modifying the Elbs reaction through catalysis and the introduction of additional oxidants, we have been able to significantly increase the yields of practically useful compounds.
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