Synthesis of chiral spirodiazafluorenes

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

[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.

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

Published print:	Nov 1, 2020
Published online:	Dec 3, 2020

Web of science	WOS:000595754000008
Scopus	2-s2.0-85097200687
Elibrary	45107758
OpenAlex	W3111010630