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Synthesis of benzo[c][1,7]naphthyridine derivatives Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 2019, Volume: 55, Number: 11, Pages: 1080-1086 Pages count : 7
Tags alkylation; benzo[c][1,7]naphthyridine; electrophilic substitution; nucleophilic substitution; oxidation; reactivity
Authors Shatsauskas Anton L. 1 , Saibulina Elina R. 2 , Gatilov Yurii V. 3,4 , Kostyuchenko Anastasia S. 1,2 , Fisyuk Alexander S. 1
Affiliations
1 Omsk State Technical University
2 Dostoevsky Omsk State University
3 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences
4 Novosibirsk State University

Abstract: Reactivity of 2-methyl-6-phenylbenzo[c][1,7]naphthyridine in alkylation, oxidation, and electrophilic substitution reactions has been studied. The reaction of 2-methyl-6-phenylbenzo[c][1,7]naphthyridines with POCl 3 yielded the previously unknown 4-chloro-2-methyl-6-phenylbenzo[c][1,7]naphthyridine. Its dehalogenation and substitution of halogen by nitrogen and sulfur nucleophiles were studied.
Cite: Shatsauskas A.L. , Saibulina E.R. , Gatilov Y.V. , Kostyuchenko A.S. , Fisyuk A.S.
Synthesis of benzo[c][1,7]naphthyridine derivatives
Chemistry of Heterocyclic Compounds. 2019. V.55. N11. P.1080-1086. WOS Scopus РИНЦ
Original: Шацаускас А.Л. , Сайбулина Э.Р. , Гатилов Ю.В. , Костюченко А.С. , Фисюк А.С.
Синтез производных бензо[c][1,7]нафтиридина
Химия гетероциклических соединений. 2019. Т.55. №11. С.1080-1086.
Dates:
Submitted: Sep 6, 2019
Accepted: Oct 2, 2019
Identifiers:
Web of science: WOS:000510838100007
Scopus: 2-s2.0-85076018018
Elibrary: 43216573
Citing:
DB Citing
Web of science 4
Scopus 6