Abstract
The corresponding carbamates were obtained by carbonylation in the presence of selenourea of benzyl- and aryl-substituted pyridines that contain a nitro group in the benzene ring and as a result of carbonylation of 7-nitro-1-azafluorene. The reaction is accompanied by simultaneous reduction of the nitro group to an amino group.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 79–81, January, 1983.
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Lapidus, A.L., Soldatenkov, A.T., Pirozhkov, S.D. et al. Catalytic carbonylation of nitrobenzyl- and nitroarylpyridines. Chem Heterocycl Compd 19, 71–73 (1983). https://doi.org/10.1007/BF00512819
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DOI: https://doi.org/10.1007/BF00512819