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Synthesis of 2,2′-quinocyanines with long N-alkyl substituents Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 2002, Volume: 38, Number: 10, Pages: 1233-1241 Pages count : 9 DOI: 10.1023/A:1021785630927
Tags 2,2′-quinocyanines; 1H NMR spectroscopy; N-alkyl groups
Authors Orlova N.A. 1 , Kolchina E.F. 1 , Zhuravlev F.A. 1 , Shakirov M.M. 1 , Gerasimova T.N. 1 , Shelkovnikov V.V. 1
Affiliations
1 (Scopus) N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russian Federation

Abstract: 2,2′-Quinocyanines with long alkyl substituents on one or both nitrogen atoms have been synthesized. 1H NMR spectroscopy has been used to study the processes occurring during the alkylation of the starting quinoline bases.
Cite: Orlova N.A. , Kolchina E.F. , Zhuravlev F.A. , Shakirov M.M. , Gerasimova T.N. , Shelkovnikov V.V.
Synthesis of 2,2′-quinocyanines with long N-alkyl substituents
Chemistry of Heterocyclic Compounds. 2002. V.38. N10. P.1233-1241. DOI: 10.1023/A:1021785630927 Scopus РИНЦ OpenAlex
Identifiers:
Scopus: 2-s2.0-0036826701
Elibrary: 13408617
OpenAlex: W2951880444
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