Alkylation of 3-methyl-1H-acenaphtho[5,6-de]pyridazine
- Авторлар: Omelichkin N.I.1, Minyaeva L.G.1, Mezheritskii V.V.1
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Мекемелер:
- Research Institute of Physical and Organic Chemistry at Southern Federal University
- Шығарылым: Том 53, № 2 (2017)
- Беттер: 258-262
- Бөлім: Article
- URL: https://journals.rcsi.science/1070-4280/article/view/215805
- DOI: https://doi.org/10.1134/S1070428017020208
- ID: 215805
Дәйексөз келтіру
Аннотация
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.
Авторлар туралы
N. Omelichkin
Research Institute of Physical and Organic Chemistry at Southern Federal University
Хат алмасуға жауапты Автор.
Email: niomelichkin@sfedu.ru
Ресей, 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
Ресей, 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
Ресей, pr. Stachki 194/2, Rostov-on-Don, 344090
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