Trifluoroacetylation of N-Substituted 1H-1,2-Diazaphenalenes of the Naphthalene and Acenaphthene Series


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Resumo

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.

Sobre autores

G. Borodkin

Research Institute of Physical and Organic Chemistry

Email: niomelichkin@sfedu.ru
Rússia, pr. Stachki 194/2, Rostov-on-Don, 344090

L. Kuz’mina

Kurnakov Institute of General and Inorganic Chemistry

Email: niomelichkin@sfedu.ru
Rússia, Leninskii pr. 31, Moscow, 119991

V. Mezheritskii

Research Institute of Physical and Organic Chemistry

Email: niomelichkin@sfedu.ru
Rússia, pr. Stachki 194/2, Rostov-on-Don, 344090

N. Omelichkin

Research Institute of Physical and Organic Chemistry

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

Email: niomelichkin@sfedu.ru
Rússia, pr. Stachki 194/2, Rostov-on-Don, 344090

M. Korobov

Research Institute of Physical and Organic Chemistry

Email: niomelichkin@sfedu.ru
Rússia, pr. Stachki 194/2, Rostov-on-Don, 344090

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