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Synthesis of chiral spirodiazafluorenes Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 2020, Volume: 56, Number: 11, Pages: 1429–1433 Pages count : DOI: 10.1007/s10593-020-02833-y
Tags chiral bipyridyls; chiral pyridines; chirality; diazafluorenes; donor-acceptor systems; electrophilic alkylation; spiro compounds; terpenes
Authors Ustimenko Yulia P. 1 , Vasilyev Eugene S. 1 , Bizyaev Sergey N. 1 , Rybalova Tatyana V. 1 , Tkachev Alexey V. 1
Affiliations
1 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 Akademika Lavrentieva Ave., Novosibirsk, 630090, Russian Federation

Abstract: [Figure not available: see fulltext.] Reactions of chiral nopinane-annulated diazafluorenone with substituted phenols and naphthols by the action of trifluoromethanesulfonic acid led to spiro products. The structure of the resorcinol derivative was confirmed by X-ray structural analysis. © 2020, Springer Science+Business Media, LLC, part of Springer Nature.
Cite: Ustimenko Y.P. , Vasilyev E.S. , Bizyaev S.N. , Rybalova T.V. , Tkachev A.V.
Synthesis of chiral spirodiazafluorenes
Chemistry of Heterocyclic Compounds. 2020. V.56. N11. P.1429–1433. DOI: 10.1007/s10593-020-02833-y WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Nov 1, 2020
Published online: Dec 3, 2020
Identifiers:
Web of science: WOS:000595754000008
Scopus: 2-s2.0-85097200687
Elibrary: 45107758
OpenAlex: W3111010630
Citing:
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Scopus 1
Web of science 2
Elibrary 2
OpenAlex 2
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