Trifluoroacetylation of N-Substituted 1H-1,2-Diazaphenalenes of the Naphthalene and Acenaphthene Series
- Авторы: Borodkin G.S.1, Kuz’mina L.G.2, Mezheritskii V.V.1, Omelichkin N.I.1, Minyaeva L.G.1, Korobov M.S.1
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Учреждения:
- Research Institute of Physical and Organic Chemistry
- Kurnakov Institute of General and Inorganic Chemistry
- Выпуск: Том 55, № 1 (2019)
- Страницы: 87-92
- Раздел: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/219731
- DOI: https://doi.org/10.1134/S107042801901010X
- ID: 219731
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Аннотация
The acylation of N-substituted 3-methyl-1H-1,2-diazaphenalenes of the naphthalene and acenaphthene series with trifluoroacetic anhydride gave mono- and diacylated products. Despite the presence of a bulky substituent on the pyrrole type nitrogen atom, the trifluoroacetyl group entered the peri position with respect to that substituent. The product structure was confirmed by X-ray analysis.
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Об авторах
G. Borodkin
Research Institute of Physical and Organic Chemistry
Email: niomelichkin@sfedu.ru
Россия, pr. Stachki 194/2, Rostov-on-Don, 344090
L. Kuz’mina
Kurnakov Institute of General and Inorganic Chemistry
Email: niomelichkin@sfedu.ru
Россия, Leninskii pr. 31, Moscow, 119991
V. Mezheritskii
Research Institute of Physical and Organic Chemistry
Email: niomelichkin@sfedu.ru
Россия, pr. Stachki 194/2, Rostov-on-Don, 344090
N. Omelichkin
Research Institute of Physical and Organic Chemistry
Автор, ответственный за переписку.
Email: niomelichkin@sfedu.ru
Россия, pr. Stachki 194/2, Rostov-on-Don, 344090
L. Minyaeva
Research Institute of Physical and Organic Chemistry
Email: niomelichkin@sfedu.ru
Россия, pr. Stachki 194/2, Rostov-on-Don, 344090
M. Korobov
Research Institute of Physical and Organic Chemistry
Email: niomelichkin@sfedu.ru
Россия, pr. Stachki 194/2, Rostov-on-Don, 344090
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