Abstract
An unusual path for the reaction of 2-aryl-1-dimethylamino-2H-isoindoles with N-R-maleimides, leading to the imides of l,2-dihydronaphthalene-2,3-dicarboxylic adds, was established by x-ray crystallographic analysis.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 614–618, May, 1992
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Kucherenko, T.T., Muzyka, P.V., Rusanov, É.B. et al. X-ray crystallographic investigation of the adduct of 1-demethylamino-2-(4-bromophenyl-2H-isoindole with N-phenylmalemide. Chem Heterocycl Compd 28, 515–518 (1992). https://doi.org/10.1007/BF00475247
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DOI: https://doi.org/10.1007/BF00475247