Enviar artigo por via de e-mail Alkylation of 3-methyl-1H-acenaphtho[5,6-de]pyridazine
- Autores: Omelichkin N.I.1, Minyaeva L.G.1, Mezheritskii V.V.1
-
Afiliações:
- Research Institute of Physical and Organic Chemistry at Southern Federal University
- Edição: Volume 53, Nº 2 (2017)
- Páginas: 258-262
- Seção: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/215805
- DOI: https://doi.org/10.1134/S1070428017020208
- ID: 215805
Citar
Acesso aberto
Acesso está concedido
Somente assinantes
Resumo
Alkylation of 3-methyl-1Н-acenaphtho[5,6]pyridazine with methyl and propyl iodides as well as with benzyl chloride in alkaline medium leads to the formation of the corresponding both N- and С-substituted pyridazine derivatives and also to the dimerization product of the initial compound. The ratio of obtained compounds depends on the used hydride, reaction temperature, and solvent.
Sobre autores
N. Omelichkin
Research Institute of Physical and Organic Chemistry at Southern Federal University
Autor responsável pela correspondência
Email: niomelichkin@sfedu.ru
Rússia, pr. Stachki 194/2, Rostov-on-Don, 344090
L. Minyaeva
Research Institute of Physical and Organic Chemistry at Southern Federal University
Email: niomelichkin@sfedu.ru
Rússia, pr. Stachki 194/2, Rostov-on-Don, 344090
V. Mezheritskii
Research Institute of Physical and Organic Chemistry at Southern Federal University
Email: niomelichkin@sfedu.ru
Rússia, pr. Stachki 194/2, Rostov-on-Don, 344090
Arquivos suplementares
