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Two Routes of Heterocyclization of 2-Alkynylanthraquinone-1-diazonium Salts. The Synthesis of 1H-Naphtho[2,3-h]cinnoline-4,7,12-trione Full article

Journal Tetrahedron
ISSN: 0040-4020 , E-ISSN: 1464-5416
Output data Year: 2001, Volume: 57, Number: 7, Pages: 1331-1334 Pages count : 4 DOI: 10.1016/S0040-4020(00)01101-7
Tags 3-Substituted naphthoindazolediones and naphthocinnolinetriones, Heterocyclization, ortho-alkynylarenediazonium salts, Richter reaction
Authors Fedenok Lidiya G. 1 , Barabanov Igor I. 1 , Ivanchikova Irena D. 1
Affiliations
1 Institute of Chemical Kinetics and Combustion, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090, Russia

Abstract: The possibility of the heterocyclization of vic-alkynylanthraquinonediazonium salts with the formation of a 5- or 6-membered ring, depending on the reaction conditions, is established. The heterocyclization of 2-alkynyl-9,10-anthraquinone-1-diazonium salts to form 1H-naphtho[2,3-h]cinnoline-4,7,12-triones is reported.
Cite: Fedenok L.G. , Barabanov I.I. , Ivanchikova I.D.
Two Routes of Heterocyclization of 2-Alkynylanthraquinone-1-diazonium Salts. The Synthesis of 1H-Naphtho[2,3-h]cinnoline-4,7,12-trione
Tetrahedron. 2001. V.57. N7. P.1331-1334. DOI: 10.1016/S0040-4020(00)01101-7 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Aug 2, 2000
Accepted: Nov 16, 2000
Published print: Feb 11, 2001
Published online: Feb 19, 2001
Identifiers:
Web of science: WOS:000166894100024
Scopus: 2-s2.0-0035843383
Elibrary: 13388448
Chemical Abstracts: 2001:118792
Chemical Abstracts (print): 134:311148
OpenAlex: W2950206134
Citing:
DB Citing
Web of science 15
Scopus 17
OpenAlex 15
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