Аннотация:
A two-stage selective synthesis of new substituted 5-hydroxypyrazolo[1,5-a]quinoxalin-4-ones from ethyl 3-arylpyrazole-5-carboxylates and activated o-chloronitroarenes substrates has been developed.
Образец цитирования:
V. A. Panova, M. K. Korsakov, A. A. Shetnev, S. I. Filimonov, “Synthesis of substituted 5-hydroxypyrazolo[1,5-a]quinoxalin-4-ones”, Mendeleev Commun., 29:1 (2019), 114–115
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