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

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

Журнал

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Вых. Данные

Год: 2002, Том: 38, Номер: 10, Страницы: 1233-1241 Страниц : 9 DOI: 10.1023/A:1021785630927

Ключевые слова

2,2′-quinocyanines; 1H NMR spectroscopy; N-alkyl groups

Авторы

Orlova N.A. ¹ , Kolchina E.F. ¹ , Zhuravlev F.A. ¹ , Shakirov M.M. ¹ , Gerasimova T.N. ¹ , Shelkovnikov V.V. ¹

Организации

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
РИНЦ	13408617
OpenAlex	W2951880444