Abstract
2,4,6-Triaryl-1,3-diazabicyclo[3.1.0]hex-3-enes were prepared by the reaction of α,Β-dibromochalcones with aromatic aldehydes and ammonia. The exo- and endo-isomers were isolated and characterized. X-ray structural analysis of the endo-6-(4-nitrophenyl)-2,4-diphenyl derivative was performed.
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See [1] for Communication 9.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1060–1066, August, 1991.
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Orlov, V.D., Kaluski, Z., Figas, É. et al. Aziridinyl ketones and their cyclic anils. 10. 2,4,6-Triaryl-1,3-diazabicyclo[3.1.0]hex-3-enes. Chem Heterocycl Compd 27, 849–854 (1991). https://doi.org/10.1007/BF00472284
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DOI: https://doi.org/10.1007/BF00472284