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Thermal transformations of 7-aryl-1,6-diazabicyclo[4.10]heptanes and 6,13-diarylperhydrodipyridazino-[1,2-a: 1′,2′-d]-1,2,4,5-tetrazines

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Abstract

The thermolysis of 7-aryl-1,6-diazabicyclo[4.1.0]heptanes in the absence of 1,3-dipolarophiles leads to dimers of the initially formed azomethineimines, namely, 6,13-diaryloctahydrodipyridazino[1,2-a:1′,2′

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Correspondence to Yu. B. Koptelov.

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Dedicated to the memory of A. A. Potekhin.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 1062–1070, July, 2008.

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Koptelov, Y.B., Ukolov, A.I. Thermal transformations of 7-aryl-1,6-diazabicyclo[4.10]heptanes and 6,13-diarylperhydrodipyridazino-[1,2-a: 1′,2′-d]-1,2,4,5-tetrazines. Chem Heterocycl Comp 44, 852–859 (2008). https://doi.org/10.1007/s10593-008-0120-7

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  • DOI: https://doi.org/10.1007/s10593-008-0120-7

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