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Synthesis and reactions of 1-aryl-3-formyl-4,6-dinitro-1H-indazoles Full article

Journal Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Output data Year: 2002, Volume: 12, Number: 5, Pages: 198-200 Pages count : 3 DOI: 10.1070/mc2002v012n05abeh001641
Authors Vinogradov Vasilii M. 1 , Starosotnikov Aleksei M. 1 , Shevelev Svyatoslav A. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Abstract: The title compounds were prepared by the reactions of picrylacetaldehyde with aryldiazonium salts followed by the intramolecular cyclization of the resulting picrylglyoxal monoarylhydrazones, and the regiospecific substitution for the nitro group at the 4-position under the action of anionic N-, O- and S-nucleophiles was found.
Cite: Vinogradov V.M. , Starosotnikov A.M. , Shevelev S.A.
Synthesis and reactions of 1-aryl-3-formyl-4,6-dinitro-1H-indazoles
Mendeleev Communications. 2002. V.12. N5. P.198-200. DOI: 10.1070/mc2002v012n05abeh001641 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000179887800015
Scopus: 2-s2.0-0036763720
OpenAlex: W1963872707
Citing:
DB Citing
OpenAlex 12
Scopus 18
Web of science 21
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