Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines

Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines Full article

Journal

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Output data

Year: 2020, Volume: 56, Number: 8, Pages: 1042-1047 Pages count : 6 DOI: 10.1007/s10593-020-02772-8

Tags

1,10-phenanthroline; 1,3-dipolar cycloaddition; acceptor alkenes; N-aminophenanthrolinium cation; pyrazolo[1,5-a][1,10]phenanthrolines

Authors

Sannikova Viktoriya А. ¹ , Filippov Igor R. ^1,2 , Karmatskikh Oleg Yu. ^1,2 , Panfilov Mikhail А. ¹ , Andreev Rodion V. ¹ , Vorob’ev Aleksey Yu. ^1,2

Affiliations

1	(Scopus) N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 Akademika Lavrentieva Ave., Novosibirsk, 630090, Russian Federation
2	(Scopus) Novosibirsk State University, 1 Pirogova St., Novosibirsk, 630090, Russian Federation

[Figure not available: see fulltext.] The reaction of N-amino-1,10-phenanthrolinium mesitylenesulfonate with acceptor-substituted alkenes in the K2CO3–DMSO system gave 3- and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines. A wide range of alkenes enter into this reaction; however, in the case of nitro derivatives, complex mixtures of products were formed. © 2020, Springer Science+Business Media, LLC, part of Springer Nature.

Sannikova V.А. , Filippov I.R. , Karmatskikh O.Y. , Panfilov M.А. , Andreev R.V. , Vorob’ev A.Y.
Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines
Chemistry of Heterocyclic Compounds. 2020. V.56. N8. P.1042-1047. DOI: 10.1007/s10593-020-02772-8 WOS Scopus РИНЦ OpenAlex

Published print:	Aug 1, 2020
Published online:	Sep 23, 2020

Web of science:	WOS:000572306400006
Scopus:	2-s2.0-85091432336
Elibrary:	45309896
OpenAlex:	W3087773791

DB	Citing
Scopus	3
Web of science	3
Elibrary	4
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