Abstract
1-Substituted 1H-1,2-diazaphenalenes (1H-benzo[de]cinnolines) undergo nitration with nitric acid leading to the formation of di- and trinitro derivatives. The yield of nitration products depends on nitric acid concentration.
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Original Russian Text © V.V. Mezeritskii, L.G. Minyaeva, N.I. Omelichkin, G.S. Borodkin, M.S. Korobov, 2015, published in Zhurnal Organicheskoi Khimii, 2015, Vol. 51, No. 5, pp. 689–692.
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Mezeritskii, V.V., Minyaeva, L.G., Omelichkin, N.I. et al. Nitration of 3-methyl-1H-1,2-diazaphenalene and its n-substituted derivatives. Russ J Org Chem 51, 670–673 (2015). https://doi.org/10.1134/S1070428015050152
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DOI: https://doi.org/10.1134/S1070428015050152