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

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

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.

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

Scopus	2-s2.0-0036826701
Elibrary	13408617
OpenAlex	W2951880444