2020
DOI: 10.1007/s11172-020-2986-1
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Synthesis of substituted pyrazolo[1,5-a]quinoxalines using the reductive cyclization

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“…Under the reaction conditions, a predominant nucleophilic substitution at the N 2 atom of the pyrazole ring was observed. Subsequent reduction of the nitro derivative with tin(II) chloride and other reagents [22] in all cases gave N-hydroxyquinoxalines as the products of reductive cyclization. The obtained compounds showed the properties of potent and selective inhibitors of human monoamine oxidase [23].…”
Section: Doi: 101134/s1070363221060049mentioning
confidence: 99%
“…Under the reaction conditions, a predominant nucleophilic substitution at the N 2 atom of the pyrazole ring was observed. Subsequent reduction of the nitro derivative with tin(II) chloride and other reagents [22] in all cases gave N-hydroxyquinoxalines as the products of reductive cyclization. The obtained compounds showed the properties of potent and selective inhibitors of human monoamine oxidase [23].…”
Section: Doi: 101134/s1070363221060049mentioning
confidence: 99%