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Reactions of highly electrophilic azolo[b]pyridines with polyphenols Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2023, Volume: 72, Number: 5, Pages: 1219-1224 Pages count : 6 DOI: 10.1007/s11172-023-3892-0
Authors Starosotnikov A.M. 1 , Bastrakov M.A. 1 , Kokorekin V.A. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Reactions of highly electrophilic azolo[b]pyridines with di- and triatomic phenols lead to products of 1,4-addition of C-nucleophiles to the pyridine cycle. It is found that another type of azoloazines, namely [1,2,4]triazolo[1,5-a]pyridines, are also capable to form adducts with polyphenols. Synthesized compounds containing simultaneously several pharmacophoric fragments are of interest as potential biologically active compounds.
Cite: Starosotnikov A.M. , Bastrakov M.A. , Kokorekin V.A.
Reactions of highly electrophilic azolo[b]pyridines with polyphenols
Russian Chemical Bulletin. 2023. V.72. N5. P.1219-1224. DOI: 10.1007/s11172-023-3892-0 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000995788300016
Scopus: 2-s2.0-85160216118
OpenAlex: W4378550089
Citing:
DB Citing
OpenAlex 5
Scopus 5
Web of science 5
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