Reactions of 9-aroyl-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8-octahydroxanthene-1,8-diones with hydrazine and methylhydrazine produced cinnoline derivatives. A homolytic cleavage of C–C bond in the intermediate product occured in the case of methylhydrazine, leading to the dimeric 4,4'-bis(3-aryl-1,7,7-trimethyl-1,4,5,6,7,8-hexahydrocinnoline-5-ones).
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This investigation was performed within the framework of the Latvian National Research Program “Development of New Preventive, Treatment, Diagnostic Means and Methods, Biomedical Technologies for Improvement of Public Health” (2010-2013).
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*Dedicated to Academician J. Stradiņš on the occasion of his 80th birthday.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1783-1787, November, 2013.
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Bisenieks, E., Uldrikis, J., Poikans, J. et al. Reactions of 9-Aroyl-3,3,6,6-Tetramethyl-1,2,3,4,5,6,7,8-Octahydroxanthene-1,8-Diones With Hydrazine and Methylhydrazine*. Chem Heterocycl Comp 49, 1653–1657 (2014). https://doi.org/10.1007/s10593-014-1416-4
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DOI: https://doi.org/10.1007/s10593-014-1416-4