Abstract:
The high reactivity of 4-bromo-5-nitrophthalonitrile and different mobilities of the leaving groups (bromo and nitro) in aromatic nucleophilic substitution reactions offer new opportunities for the synthesis of substituted phthalonitriles and then various heterocyclic compounds.
Document Type:
Article
Language: English
Citation:
I. G. Abramov, M. V. Dorogov, S. A. Ivanovskii, A. V. Smirnov, M. B. Abramova, “The differing reactivity of the bromo and nitro groups in 4-bromo-5-nitrophthalonitrile towards nucleophilic attack”, Mendeleev Commun., 10:2 (2000), 78–80
Linking options:
https://www.mathnet.ru/eng/mendc4393
https://www.mathnet.ru/eng/mendc/v10/i2/p78
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